Canonical Allele Identifier: CA8560487

Gene: KRT13

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41502401C>A , CM000679.2:g.41502401C>A	GRCh38
NC_000017.10:g.39658653C>A , CM000679.1:g.39658653C>A	GRCh37
NC_000017.9:g.36912179C>A	NCBI36
NG_008406.1:g.8213G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_153490.3:c.1217G>T MANE Select	NP_705694.3:p.Arg406Leu
ENST00000246635.8:c.1217G>T MANE Select	ENSP00000246635.3:p.Arg406Leu
NM_002274.3:c.1217G>T	NP_002265.2:p.Arg406Leu
NM_002274.4:c.1217G>T	NP_002265.3:p.Arg406Leu
NM_153490.2:c.1217G>T	NP_705694.2:p.Arg406Leu
ENST00000246635.7:c.1217G>T	ENSP00000246635.3:p.Arg406Leu
ENST00000336861.7:c.1217G>T	ENSP00000336604.3:p.Arg406Leu
ENST00000464634.2:c.*814G>T	ENSP00000466525.1:n.*814G>T
ENST00000468313.5:n.1053G>T
ENST00000587544.5:c.1217G>T	ENSP00000468221.1:p.Arg406Leu