Canonical Allele Identifier: CA343772214
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873080G>T (hg19) chr1:g.173903942G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903942G>T , CM000663.2:g.173903942G>T GRCh38
NC_000001.10:g.173873080G>T , CM000663.1:g.173873080G>T GRCh37
NC_000001.9:g.172139703G>T NCBI36
NG_012462.1:g.18437C>A , LRG_577:g.18437C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1342C>A MANE Select ENSP00000356671.3:p.Pro448Thr
ENST00000367698.3:c.1342C>A ENSP00000356671.3:p.Pro448Thr
ENST00000617423.4:c.727C>A ENSP00000478688.1:p.Pro243Thr
NM_000488.3:c.1342C>A , LRG_577t1:c.1342C>A NP_000479.1:p.Pro448Thr
XM_005245198.2:c.1198C>A XP_005245255.1:p.Pro400Thr
NM_001365052.1:c.1198C>A NP_001351981.1:p.Pro400Thr
NM_000488.4:c.1342C>A MANE Select NP_000479.1:p.Pro448Thr
NM_001365052.2:c.1198C>A NP_001351981.1:p.Pro400Thr
NM_001386302.1:c.1465C>A NP_001373231.1:p.Pro489Thr
NM_001386303.1:c.1423C>A NP_001373232.1:p.Pro475Thr
NM_001386304.1:c.1321C>A NP_001373233.1:p.Pro441Thr
NM_001386305.1:c.1285C>A NP_001373234.1:p.Pro429Thr
NM_001386306.1:c.1126C>A NP_001373235.1:p.Pro376Thr
Search 100 bp 5'
Search 100 bp 3'