Canonical Allele Identifier: CA1207937651
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1657764230

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173911386_173911387del , CM000663.2:g.173911386_173911387del GRCh38
NC_000001.10:g.173880524_173880525del , CM000663.1:g.173880524_173880525del GRCh37
NC_000001.9:g.172147147_172147148del NCBI36
NG_012462.1:g.10994_10995del , LRG_577:g.10994_10995del

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.624+414_624+415del MANE Select ENSP00000356671.3:n.624+414_624+415del
ENST00000367698.3:c.624+414_624+415del ENSP00000356671.3:n.624+414_624+415del
ENST00000487183.1:n.329+414_329+415del
ENST00000617423.4:c.559+479_559+480del ENSP00000478688.1:n.559+479_559+480del
NM_000488.3:c.624+414_624+415del , LRG_577t1:c.624+414_624+415del NP_000479.1:n.624+414_624+415del
XM_005245198.2:c.480+414_480+415del XP_005245255.1:n.480+414_480+415del
NM_001365052.1:c.480+414_480+415del NP_001351981.1:n.480+414_480+415del
NM_000488.4:c.624+414_624+415del MANE Select NP_000479.1:n.624+414_624+415del
NM_001365052.2:c.480+414_480+415del NP_001351981.1:n.480+414_480+415del
NM_001386302.1:c.624+414_624+415del NP_001373231.1:n.624+414_624+415del
NM_001386303.1:c.705+414_705+415del NP_001373232.1:n.705+414_705+415del
NM_001386304.1:c.624+414_624+415del NP_001373233.1:n.624+414_624+415del
NM_001386305.1:c.624+414_624+415del NP_001373234.1:n.624+414_624+415del
NM_001386306.1:c.409-494_409-493del NP_001373235.1:n.409-494_409-493del