Canonical Allele Identifier: CA500206746

Gene: KRT17

Linked Data

• ClinVar Variation Id: 3053207
• ClinVar RCV Id: RCV003963821
• gnomAD v4: 17-41624402-A-G
• MyVariant Identifiers: chr17:g.39780654A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624402A>G , CM000679.2:g.41624402A>G	GRCh38
NC_000017.10:g.39780654A>G , CM000679.1:g.39780654A>G	GRCh37
NC_000017.9:g.37034180A>G	NCBI36
NG_008625.1:g.5229T>C
NG_009090.2:g.167311T>C , LRG_401:g.167311T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.108T>C MANE Select	ENSP00000308452.8:p.Gly36=
ENST00000311208.12:c.108T>C	ENSP00000308452.8:p.Gly36=
ENST00000463128.5:c.-312-196T>C	ENSP00000468672.1:n.-312-196T>C
ENST00000491673.1:n.174T>C
ENST00000540235.5:c.-98T>C	ENSP00000441751.2:n.-98T>C
ENST00000577817.3:c.63T>C	ENSP00000467418.1:p.Gly21=
NM_000422.2:c.108T>C	NP_000413.1:p.Gly36=
NM_000422.3:c.108T>C MANE Select	NP_000413.1:p.Gly36=