Canonical Allele Identifier: CA2260105524

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624328T= , CM000679.2:g.41624328T=	GRCh38
NC_000017.10:g.39780580T= , CM000679.1:g.39780580T=	GRCh37
NC_000017.9:g.37034106T=	NCBI36
NG_008625.1:g.5303A=
NG_009090.2:g.167385A= , LRG_401:g.167385A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.182A= MANE Select	ENSP00000308452.8:p.Tyr61=
ENST00000311208.12:c.182A=	ENSP00000308452.8:p.Tyr61=
ENST00000463128.5:c.-312-122A=	ENSP00000468672.1:n.-312-122A=
ENST00000491673.1:n.248A=
ENST00000540235.5:c.-24A=	ENSP00000441751.2:n.-24A=
ENST00000577817.3:c.137A=	ENSP00000467418.1:p.Tyr46=
NM_000422.2:c.182A=	NP_000413.1:p.Tyr61=
NM_000422.3:c.182A= MANE Select	NP_000413.1:p.Tyr61=