Canonical Allele Identifier: CA2637772727

Gene: KRT12

Linked Data

• gnomAD v4: 17-40866967-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40866969del , CM000679.2:g.40866969del	GRCh38
NC_000017.10:g.39023221del , CM000679.1:g.39023221del	GRCh37
NC_000017.9:g.36276747del	NCBI36
NG_008077.1:g.5243del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251643.5:c.219del MANE Select	ENSP00000251643.4:p.Gly74GlufsTer?
ENST00000647902.1:c.211+8del	ENSP00000497770.1:n.211+8del
ENST00000251643.4:c.219del	ENSP00000251643.4:p.Gly74GlufsTer?
NM_000223.3:c.219del	NP_000214.1:p.Gly74GlufsTer?
XR_934754.1:n.1500+16109del
XR_934754.2:n.2008+16109del
NM_000223.4:c.219del MANE Select	NP_000214.1:p.Gly74GlufsTer?