Canonical Allele Identifier: CA2586967700
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903927dup , CM000663.2:g.173903927dup GRCh38
NC_000001.10:g.173873065dup , CM000663.1:g.173873065dup GRCh37
NC_000001.9:g.172139688dup NCBI36
NG_012462.1:g.18452dup , LRG_577:g.18452dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1357dup MANE Select ENSP00000356671.3:p.Ile453AsnfsTer12
ENST00000367698.3:c.1357dup ENSP00000356671.3:p.Ile453AsnfsTer12
ENST00000617423.4:c.742dup ENSP00000478688.1:p.Ile248AsnfsTer12
NM_000488.3:c.1357dup , LRG_577t1:c.1357dup NP_000479.1:p.Ile453AsnfsTer12
XM_005245198.2:c.1213dup XP_005245255.1:p.Ile405AsnfsTer12
NM_001365052.1:c.1213dup NP_001351981.1:p.Ile405AsnfsTer12
NM_000488.4:c.1357dup MANE Select NP_000479.1:p.Ile453AsnfsTer12
NM_001365052.2:c.1213dup NP_001351981.1:p.Ile405AsnfsTer12
NM_001386302.1:c.1480dup NP_001373231.1:p.Ile494AsnfsTer12
NM_001386303.1:c.1438dup NP_001373232.1:p.Ile480AsnfsTer12
NM_001386304.1:c.1336dup NP_001373233.1:p.Ile446AsnfsTer12
NM_001386305.1:c.1300dup NP_001373234.1:p.Ile434AsnfsTer12
NM_001386306.1:c.1141dup NP_001373235.1:p.Ile381AsnfsTer12