Canonical Allele Identifier: CA2809477251

Gene: KRT12

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40866980_40866981insC , CM000679.2:g.40866980_40866981insC	GRCh38
NC_000017.10:g.39023232_39023233insC , CM000679.1:g.39023232_39023233insC	GRCh37
NC_000017.9:g.36276758_36276759insC	NCBI36
NG_008077.1:g.5230_5231insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251643.5:c.206_207insG MANE Select	ENSP00000251643.4:p.Phe69LeufsTer25
ENST00000647902.1:c.206_207insG	ENSP00000497770.1:p.Phe69LeufsTer13
ENST00000251643.4:c.206_207insG	ENSP00000251643.4:p.Phe69LeufsTer25
NM_000223.3:c.206_207insG	NP_000214.1:p.Phe69LeufsTer25
XR_934754.1:n.1500+16120_1500+16121insC
XR_934754.2:n.2008+16120_2008+16121insC
NM_000223.4:c.206_207insG MANE Select	NP_000214.1:p.Phe69LeufsTer25