Canonical Allele Identifier: CA2260105632

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624508A= , CM000679.2:g.41624508A=	GRCh38
NC_000017.10:g.39780760A= , CM000679.1:g.39780760A=	GRCh37
NC_000017.9:g.37034286A=	NCBI36
NG_008625.1:g.5123T=
NG_009090.2:g.167205T= , LRG_401:g.167205T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.2T= MANE Select	ENSP00000308452.8:p.Met1=
ENST00000311208.12:c.2T=	ENSP00000308452.8:p.Met1=
ENST00000463128.5:c.-313+235T=	ENSP00000468672.1:n.-313+235T=
ENST00000491673.1:n.68T=
ENST00000540235.5:c.-204T=	ENSP00000441751.2:n.-204T=
NM_000422.2:c.2T=	NP_000413.1:p.Met1=
NM_000422.3:c.2T= MANE Select	NP_000413.1:p.Met1=