Canonical Allele Identifier: CA2649174129
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903892_173903895dup , CM000663.2:g.173903892_173903895dup GRCh38
NC_000001.10:g.173873030_173873033dup , CM000663.1:g.173873030_173873033dup GRCh37
NC_000001.9:g.172139653_172139656dup NCBI36
NG_012462.1:g.18487_18490dup , LRG_577:g.18487_18490dup

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1392_1395dup MANE Select ENSP00000356671.3:n.1392_1395dup
ENST00000367698.3:c.1392_1395dup ENSP00000356671.3:n.1392_1395dup
ENST00000617423.4:c.777_780dup ENSP00000478688.1:n.777_780dup
NM_000488.3:c.1392_1395dup , LRG_577t1:c.1392_1395dup NP_000479.1:n.1392_1395dup
XM_005245198.2:c.1248_1251dup XP_005245255.1:n.1248_1251dup
NM_001365052.1:c.1248_1251dup NP_001351981.1:n.1248_1251dup
NM_000488.4:c.1392_1395dup MANE Select NP_000479.1:n.1392_1395dup
NM_001365052.2:c.1248_1251dup NP_001351981.1:n.1248_1251dup
NM_001386302.1:c.1515_1518dup NP_001373231.1:n.1515_1518dup
NM_001386303.1:c.1473_1476dup NP_001373232.1:n.1473_1476dup
NM_001386304.1:c.1371_1374dup NP_001373233.1:n.1371_1374dup
NM_001386305.1:c.1335_1338dup NP_001373234.1:n.1335_1338dup
NM_001386306.1:c.1176_1179dup NP_001373235.1:n.1176_1179dup