Canonical Allele Identifier: CA343772235
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873083C>A (hg19) chr1:g.173903945C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903945C>A , CM000663.2:g.173903945C>A GRCh38
NC_000001.10:g.173873083C>A , CM000663.1:g.173873083C>A GRCh37
NC_000001.9:g.172139706C>A NCBI36
NG_012462.1:g.18434G>T , LRG_577:g.18434G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1339G>T MANE Select ENSP00000356671.3:p.Val447Phe
ENST00000367698.3:c.1339G>T ENSP00000356671.3:p.Val447Phe
ENST00000617423.4:c.724G>T ENSP00000478688.1:p.Val242Phe
NM_000488.3:c.1339G>T , LRG_577t1:c.1339G>T NP_000479.1:p.Val447Phe
XM_005245198.2:c.1195G>T XP_005245255.1:p.Val399Phe
NM_001365052.1:c.1195G>T NP_001351981.1:p.Val399Phe
NM_000488.4:c.1339G>T MANE Select NP_000479.1:p.Val447Phe
NM_001365052.2:c.1195G>T NP_001351981.1:p.Val399Phe
NM_001386302.1:c.1462G>T NP_001373231.1:p.Val488Phe
NM_001386303.1:c.1420G>T NP_001373232.1:p.Val474Phe
NM_001386304.1:c.1318G>T NP_001373233.1:p.Val440Phe
NM_001386305.1:c.1282G>T NP_001373234.1:p.Val428Phe
NM_001386306.1:c.1123G>T NP_001373235.1:p.Val375Phe
Search 100 bp 5'
Search 100 bp 3'