Canonical Allele Identifier: CA399511695

Gene: KRT17

Linked Data

• dbSNP Id: rs1443634942
• gnomAD v3: 17-41624112-T-C
• gnomAD v4: 17-41624112-T-C
• MyVariant Identifiers: chr17:g.39780364T>C (hg19) ; chr17:g.41624112T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624112T>C , CM000679.2:g.41624112T>C	GRCh38
NC_000017.10:g.39780364T>C , CM000679.1:g.39780364T>C	GRCh37
NC_000017.9:g.37033890T>C	NCBI36
NG_008625.1:g.5519A>G
NG_009090.2:g.167601A>G , LRG_401:g.167601A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.398A>G MANE Select	ENSP00000308452.8:p.Gln133Arg
ENST00000311208.12:c.398A>G	ENSP00000308452.8:p.Gln133Arg
ENST00000463128.5:c.-218A>G	ENSP00000468672.1:n.-218A>G
ENST00000491673.1:n.464A>G
ENST00000493253.5:n.185A>G
ENST00000540235.5:c.149A>G	ENSP00000441751.2:p.Gln50Arg
ENST00000577817.3:c.353A>G	ENSP00000467418.1:p.Gln118Arg
NM_000422.2:c.398A>G	NP_000413.1:p.Gln133Arg
NM_000422.3:c.398A>G MANE Select	NP_000413.1:p.Gln133Arg