Canonical Allele Identifier: CA1251428
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs536867254

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173914527dup , CM000663.2:g.173914527dup GRCh38
NC_000001.10:g.173883665dup , CM000663.1:g.173883665dup GRCh37
NC_000001.9:g.172150288dup NCBI36
NG_012462.1:g.7853dup , LRG_577:g.7853dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.408+27dup MANE Select ENSP00000356671.3:n.408+27dup
ENST00000367698.3:c.408+27dup ENSP00000356671.3:n.408+27dup
ENST00000487183.1:n.113+27dup
ENST00000494024.1:n.634+27dup
ENST00000617423.4:c.408+27dup ENSP00000478688.1:n.408+27dup
NM_000488.3:c.408+27dup , LRG_577t1:c.408+27dup NP_000479.1:n.408+27dup
XM_005245198.2:c.264+27dup XP_005245255.1:n.264+27dup
NM_001365052.1:c.264+27dup NP_001351981.1:n.264+27dup
NM_000488.4:c.408+27dup MANE Select NP_000479.1:n.408+27dup
NM_001365052.2:c.264+27dup NP_001351981.1:n.264+27dup
NM_001386302.1:c.408+27dup NP_001373231.1:n.408+27dup
NM_001386303.1:c.489+27dup NP_001373232.1:n.489+27dup
NM_001386304.1:c.408+27dup NP_001373233.1:n.408+27dup
NM_001386305.1:c.408+27dup NP_001373234.1:n.408+27dup
NM_001386306.1:c.408+27dup NP_001373235.1:n.408+27dup