Canonical Allele Identifier: CA2260105530

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624341A= , CM000679.2:g.41624341A=	GRCh38
NC_000017.10:g.39780593A= , CM000679.1:g.39780593A=	GRCh37
NC_000017.9:g.37034119A=	NCBI36
NG_008625.1:g.5290T=
NG_009090.2:g.167372T= , LRG_401:g.167372T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.169T= MANE Select	ENSP00000308452.8:p.Tyr57=
ENST00000311208.12:c.169T=	ENSP00000308452.8:p.Tyr57=
ENST00000463128.5:c.-312-135T=	ENSP00000468672.1:n.-312-135T=
ENST00000491673.1:n.235T=
ENST00000540235.5:c.-37T=	ENSP00000441751.2:n.-37T=
ENST00000577817.3:c.124T=	ENSP00000467418.1:p.Tyr42=
NM_000422.2:c.169T=	NP_000413.1:p.Tyr57=
NM_000422.3:c.169T= MANE Select	NP_000413.1:p.Tyr57=