Canonical Allele Identifier: CA399485895

Gene: KRT13

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41503713T>A , CM000679.2:g.41503713T>A	GRCh38
NC_000017.10:g.39659965T>A , CM000679.1:g.39659965T>A	GRCh37
NC_000017.9:g.36913491T>A	NCBI36
NG_008406.1:g.6901A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_153490.3:c.508A>T MANE Select	NP_705694.3:p.Thr170Ser
ENST00000246635.8:c.508A>T MANE Select	ENSP00000246635.3:p.Thr170Ser
NM_002274.3:c.508A>T	NP_002265.2:p.Thr170Ser
NM_002274.4:c.508A>T	NP_002265.3:p.Thr170Ser
NM_153490.2:c.508A>T	NP_705694.2:p.Thr170Ser
ENST00000246635.7:c.508A>T	ENSP00000246635.3:p.Thr170Ser
ENST00000336861.7:c.508A>T	ENSP00000336604.3:p.Thr170Ser
ENST00000464634.2:c.*105A>T	ENSP00000466525.1:n.*105A>T
ENST00000468313.5:n.344A>T
ENST00000587118.1:n.525A>T
ENST00000587435.1:c.400-370A>T	ENSP00000467833.1:n.400-370A>T
ENST00000587544.5:c.508A>T	ENSP00000468221.1:p.Thr170Ser
ENST00000590425.1:c.187A>T	ENSP00000466465.1:p.Thr63Ser