Canonical Allele Identifier: CA399487034

Gene: KRT13

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41505195A>T , CM000679.2:g.41505195A>T	GRCh38
NC_000017.10:g.39661447A>T , CM000679.1:g.39661447A>T	GRCh37
NC_000017.9:g.36914973A>T	NCBI36
NG_008406.1:g.5419T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246635.8:c.356T>A MANE Select	ENSP00000246635.3:p.Leu119Gln
ENST00000246635.7:c.356T>A	ENSP00000246635.3:p.Leu119Gln
ENST00000336861.7:c.356T>A	ENSP00000336604.3:p.Leu119Gln
ENST00000464634.2:c.145T>A	ENSP00000466525.1:p.Trp49Arg
ENST00000468313.5:n.192T>A
ENST00000587435.1:c.356T>A	ENSP00000467833.1:p.Leu119Gln
ENST00000587544.5:c.356T>A	ENSP00000468221.1:p.Leu119Gln
ENST00000590425.1:c.35T>A	ENSP00000466465.1:p.Leu12Gln
NM_002274.3:c.356T>A	NP_002265.2:p.Leu119Gln
NM_153490.2:c.356T>A	NP_705694.2:p.Leu119Gln
NM_153490.3:c.356T>A MANE Select	NP_705694.3:p.Leu119Gln
NM_002274.4:c.356T>A	NP_002265.3:p.Leu119Gln