Canonical Allele Identifier: CA646271017
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903874_173903875insG , CM000663.2:g.173903874_173903875insG GRCh38
NC_000001.10:g.173873012_173873013insG , CM000663.1:g.173873012_173873013insG GRCh37
NC_000001.9:g.172139635_172139636insG NCBI36
NG_012462.1:g.18504_18505insC , LRG_577:g.18504_18505insC

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.*14_*15insC MANE Select ENSP00000356671.3:n.*14_*15insC
ENST00000367698.3:c.*14_*15insC ENSP00000356671.3:n.*14_*15insC
ENST00000617423.4:c.*14_*15insC ENSP00000478688.1:n.*14_*15insC
NM_000488.3:c.*14_*15insC , LRG_577t1:c.*14_*15insC NP_000479.1:n.*14_*15insC
XM_005245198.2:c.*14_*15insC XP_005245255.1:n.*14_*15insC
NM_001365052.1:c.*14_*15insC NP_001351981.1:n.*14_*15insC
NM_000488.4:c.*14_*15insC MANE Select NP_000479.1:n.*14_*15insC
NM_001365052.2:c.*14_*15insC NP_001351981.1:n.*14_*15insC
NM_001386302.1:c.*14_*15insC NP_001373231.1:n.*14_*15insC
NM_001386303.1:c.*14_*15insC NP_001373232.1:n.*14_*15insC
NM_001386304.1:c.*14_*15insC NP_001373233.1:n.*14_*15insC
NM_001386305.1:c.*14_*15insC NP_001373234.1:n.*14_*15insC
NM_001386306.1:c.*14_*15insC NP_001373235.1:n.*14_*15insC