Canonical Allele Identifier: CA2618946522

Gene: KRT2

Linked Data

• gnomAD v4: 12-52652110-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52652112del , CM000674.2:g.52652112del	GRCh38
NC_000012.11:g.53045896del , CM000674.1:g.53045896del	GRCh37
NC_000012.10:g.51332163del	NCBI36
NG_008296.1:g.5065del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309680.4:c.32del MANE Select	ENSP00000310861.3:p.Gly11GlufsTer?
ENST00000309680.3:c.32del	ENSP00000310861.3:p.Gly11GlufsTer?
NM_000423.2:c.32del	NP_000414.2:p.Gly11GlufsTer?
NM_000423.3:c.32del MANE Select	NP_000414.2:p.Gly11GlufsTer?