Canonical Allele Identifier: CA500206220

Gene: KRT17

Linked Data

• dbSNP Id: rs1908643386
• gnomAD v3: 17-41624159-A-G
• gnomAD v4: 17-41624159-A-G
• MyVariant Identifiers: chr17:g.39780411A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624159A>G , CM000679.2:g.41624159A>G	GRCh38
NC_000017.10:g.39780411A>G , CM000679.1:g.39780411A>G	GRCh37
NC_000017.9:g.37033937A>G	NCBI36
NG_008625.1:g.5472T>C
NG_009090.2:g.167554T>C , LRG_401:g.167554T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.351T>C MANE Select	ENSP00000308452.8:p.Arg117=
ENST00000311208.12:c.351T>C	ENSP00000308452.8:p.Arg117=
ENST00000463128.5:c.-265T>C	ENSP00000468672.1:n.-265T>C
ENST00000491673.1:n.417T>C
ENST00000493253.5:n.138T>C
ENST00000540235.5:c.102T>C	ENSP00000441751.2:p.Arg34=
ENST00000577817.3:c.306T>C	ENSP00000467418.1:p.Arg102=
NM_000422.2:c.351T>C	NP_000413.1:p.Arg117=
NM_000422.3:c.351T>C MANE Select	NP_000413.1:p.Arg117=