Canonical Allele Identifier: CA1009277544
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1657698232

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909953del , CM000663.2:g.173909953del GRCh38
NC_000001.10:g.173879091del , CM000663.1:g.173879091del GRCh37
NC_000001.9:g.172145714del NCBI36
NG_012462.1:g.12427del , LRG_577:g.12427del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.763-10del MANE Select ENSP00000356671.3:n.763-10del
ENST00000367698.3:c.763-10del ENSP00000356671.3:n.763-10del
ENST00000487183.1:n.414-10del
ENST00000617423.4:c.559+1912del ENSP00000478688.1:n.559+1912del
NM_000488.3:c.763-10del , LRG_577t1:c.763-10del NP_000479.1:n.763-10del
XM_005245198.2:c.619-10del XP_005245255.1:n.619-10del
NM_001365052.1:c.619-10del NP_001351981.1:n.619-10del
NM_000488.4:c.763-10del MANE Select NP_000479.1:n.763-10del
NM_001365052.2:c.619-10del NP_001351981.1:n.619-10del
NM_001386302.1:c.886-10del NP_001373231.1:n.886-10del
NM_001386303.1:c.844-10del NP_001373232.1:n.844-10del
NM_001386304.1:c.742-10del NP_001373233.1:n.742-10del
NM_001386305.1:c.763-67del NP_001373234.1:n.763-67del
NM_001386306.1:c.547-10del NP_001373235.1:n.547-10del