Canonical Allele Identifier: CA8560652

Gene: KRT13

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41503068C>T , CM000679.2:g.41503068C>T	GRCh38
NC_000017.10:g.39659320C>T , CM000679.1:g.39659320C>T	GRCh37
NC_000017.9:g.36912846C>T	NCBI36
NG_008406.1:g.7546G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_153490.3:c.766G>A MANE Select	NP_705694.3:p.Gly256Ser
ENST00000246635.8:c.766G>A MANE Select	ENSP00000246635.3:p.Gly256Ser
NM_002274.3:c.766G>A	NP_002265.2:p.Gly256Ser
NM_002274.4:c.766G>A	NP_002265.3:p.Gly256Ser
NM_153490.2:c.766G>A	NP_705694.2:p.Gly256Ser
ENST00000246635.7:c.766G>A	ENSP00000246635.3:p.Gly256Ser
ENST00000336861.7:c.766G>A	ENSP00000336604.3:p.Gly256Ser
ENST00000464634.2:c.*363G>A	ENSP00000466525.1:n.*363G>A
ENST00000468313.5:n.602G>A
ENST00000587544.5:c.766G>A	ENSP00000468221.1:p.Gly256Ser
ENST00000590425.1:c.445G>A	ENSP00000466465.1:p.Gly149Ser