Canonical Allele Identifier: CA399513061

Gene: KRT17

Linked Data

• dbSNP Id: rs1421493202
• gnomAD v3: 17-41624321-A-T
• gnomAD v4: 17-41624321-A-T
• MyVariant Identifiers: chr17:g.39780573A>T (hg19) ; chr17:g.41624321A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624321A>T , CM000679.2:g.41624321A>T	GRCh38
NC_000017.10:g.39780573A>T , CM000679.1:g.39780573A>T	GRCh37
NC_000017.9:g.37034099A>T	NCBI36
NG_008625.1:g.5310T>A
NG_009090.2:g.167392T>A , LRG_401:g.167392T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.189T>A MANE Select	ENSP00000308452.8:p.Phe63Leu
ENST00000311208.12:c.189T>A	ENSP00000308452.8:p.Phe63Leu
ENST00000463128.5:c.-312-115T>A	ENSP00000468672.1:n.-312-115T>A
ENST00000491673.1:n.255T>A
ENST00000540235.5:c.-17T>A	ENSP00000441751.2:n.-17T>A
ENST00000577817.3:c.144T>A	ENSP00000467418.1:p.Phe48Leu
NM_000422.2:c.189T>A	NP_000413.1:p.Phe63Leu
NM_000422.3:c.189T>A MANE Select	NP_000413.1:p.Phe63Leu