Canonical Allele Identifier: CA1207937051
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909938_173909939delinsAG , CM000663.2:g.173909938_173909939delinsAG GRCh38
NC_000001.10:g.173879076_173879077delinsAG , CM000663.1:g.173879076_173879077delinsAG GRCh37
NC_000001.9:g.172145699_172145700delinsAG NCBI36
NG_012462.1:g.12440_12441delinsCT , LRG_577:g.12440_12441delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.766_767delinsCT MANE Select ENSP00000356671.3:p.Leu256=
ENST00000367698.3:c.766_767delinsCT ENSP00000356671.3:p.Leu256=
ENST00000487183.1:n.417_418delinsCT
ENST00000617423.4:c.559+1925_559+1926delinsCT ENSP00000478688.1:n.559+1925_559+1926delinsCT
NM_000488.3:c.766_767delinsCT , LRG_577t1:c.766_767delinsCT NP_000479.1:p.Leu256=
XM_005245198.2:c.622_623delinsCT XP_005245255.1:p.Leu208=
NM_001365052.1:c.622_623delinsCT NP_001351981.1:p.Leu208=
NM_000488.4:c.766_767delinsCT MANE Select NP_000479.1:p.Leu256=
NM_001365052.2:c.622_623delinsCT NP_001351981.1:p.Leu208=
NM_001386302.1:c.889_890delinsCT NP_001373231.1:p.Leu297=
NM_001386303.1:c.847_848delinsCT NP_001373232.1:p.Leu283=
NM_001386304.1:c.745_746delinsCT NP_001373233.1:p.Leu249=
NM_001386305.1:c.763-54_763-53delinsCT NP_001373234.1:n.763-54_763-53delinsCT
NM_001386306.1:c.550_551delinsCT NP_001373235.1:p.Leu184=