Canonical Allele Identifier: CA399513793

Gene: KRT17

Linked Data

• dbSNP Id: rs1387497386
• gnomAD v3: 17-41624446-C-G
• gnomAD v4: 17-41624446-C-G
• MyVariant Identifiers: chr17:g.39780698C>G (hg19) ; chr17:g.41624446C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624446C>G , CM000679.2:g.41624446C>G	GRCh38
NC_000017.10:g.39780698C>G , CM000679.1:g.39780698C>G	GRCh37
NC_000017.9:g.37034224C>G	NCBI36
NG_008625.1:g.5185G>C
NG_009090.2:g.167267G>C , LRG_401:g.167267G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.64G>C MANE Select	ENSP00000308452.8:p.Gly22Arg
ENST00000311208.12:c.64G>C	ENSP00000308452.8:p.Gly22Arg
ENST00000463128.5:c.-312-240G>C	ENSP00000468672.1:n.-312-240G>C
ENST00000491673.1:n.130G>C
ENST00000540235.5:c.-142G>C	ENSP00000441751.2:n.-142G>C
ENST00000577817.3:c.19G>C	ENSP00000467418.1:p.Gly7Arg
NM_000422.2:c.64G>C	NP_000413.1:p.Gly22Arg
NM_000422.3:c.64G>C MANE Select	NP_000413.1:p.Gly22Arg