Canonical Allele Identifier: CA399512728

Gene: KRT17

Linked Data

• dbSNP Id: rs1313304776
• MyVariant Identifiers: chr17:g.39780523A>G (hg19) ; chr17:g.41624271A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624271A>G , CM000679.2:g.41624271A>G	GRCh38
NC_000017.10:g.39780523A>G , CM000679.1:g.39780523A>G	GRCh37
NC_000017.9:g.37034049A>G	NCBI36
NG_008625.1:g.5360T>C
NG_009090.2:g.167442T>C , LRG_401:g.167442T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.239T>C MANE Select	ENSP00000308452.8:p.Leu80Pro
ENST00000311208.12:c.239T>C	ENSP00000308452.8:p.Leu80Pro
ENST00000463128.5:c.-312-65T>C	ENSP00000468672.1:n.-312-65T>C
ENST00000491673.1:n.305T>C
ENST00000493253.5:n.26T>C
ENST00000540235.5:c.34T>C	ENSP00000441751.2:p.Trp12Arg
ENST00000577817.3:c.194T>C	ENSP00000467418.1:p.Leu65Pro
NM_000422.2:c.239T>C	NP_000413.1:p.Leu80Pro
NM_000422.3:c.239T>C MANE Select	NP_000413.1:p.Leu80Pro