Canonical Allele Identifier: CA2260105686

Gene: KRT17

Linked Data

• dbSNP Id: rs1908668265

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624573T>C , CM000679.2:g.41624573T>C	GRCh38
NC_000017.10:g.39780825T>C , CM000679.1:g.39780825T>C	GRCh37
NC_000017.9:g.37034351T>C	NCBI36
NG_008625.1:g.5058A>G
NG_009090.2:g.167140A>G , LRG_401:g.167140A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.-64A>G MANE Select	ENSP00000308452.8:n.-64A>G
ENST00000311208.12:c.-64A>G	ENSP00000308452.8:n.-64A>G
ENST00000463128.5:c.-313+170A>G	ENSP00000468672.1:n.-313+170A>G
ENST00000491673.1:n.3A>G
NM_000422.2:c.-64A>G	NP_000413.1:n.-64A>G
NM_000422.3:c.-64A>G MANE Select	NP_000413.1:n.-64A>G