Canonical Allele Identifier: CA2260105619

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624490T= , CM000679.2:g.41624490T=	GRCh38
NC_000017.10:g.39780742T= , CM000679.1:g.39780742T=	GRCh37
NC_000017.9:g.37034268T=	NCBI36
NG_008625.1:g.5141A=
NG_009090.2:g.167223A= , LRG_401:g.167223A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.20A= MANE Select	ENSP00000308452.8:p.Gln7=
ENST00000311208.12:c.20A=	ENSP00000308452.8:p.Gln7=
ENST00000463128.5:c.-313+253A=	ENSP00000468672.1:n.-313+253A=
ENST00000491673.1:n.86A=
ENST00000540235.5:c.-186A=	ENSP00000441751.2:n.-186A=
NM_000422.2:c.20A=	NP_000413.1:p.Gln7=
NM_000422.3:c.20A= MANE Select	NP_000413.1:p.Gln7=