Canonical Allele Identifier: CA2260105624

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624496A= , CM000679.2:g.41624496A=	GRCh38
NC_000017.10:g.39780748A= , CM000679.1:g.39780748A=	GRCh37
NC_000017.9:g.37034274A=	NCBI36
NG_008625.1:g.5135T=
NG_009090.2:g.167217T= , LRG_401:g.167217T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.14T= MANE Select	ENSP00000308452.8:p.Ile5=
ENST00000311208.12:c.14T=	ENSP00000308452.8:p.Ile5=
ENST00000463128.5:c.-313+247T=	ENSP00000468672.1:n.-313+247T=
ENST00000491673.1:n.80T=
ENST00000540235.5:c.-192T=	ENSP00000441751.2:n.-192T=
NM_000422.2:c.14T=	NP_000413.1:p.Ile5=
NM_000422.3:c.14T= MANE Select	NP_000413.1:p.Ile5=