Canonical Allele Identifier: CA626018292

Gene: KRT17

Linked Data

• dbSNP Id: rs1287545965
• gnomAD v2: 17-39780066-A-G
• gnomAD v3: 17-41623814-A-G
• gnomAD v4: 17-41623814-A-G
• MyVariant Identifiers: chr17:g.39780066A>G (hg19) ; chr17:g.41623814A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41623814A>G , CM000679.2:g.41623814A>G	GRCh38
NC_000017.10:g.39780066A>G , CM000679.1:g.39780066A>G	GRCh37
NC_000017.9:g.37033592A>G	NCBI36
NG_008625.1:g.5817T>C
NG_009090.2:g.167899T>C , LRG_401:g.167899T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.432+264T>C MANE Select	ENSP00000308452.8:n.432+264T>C
ENST00000311208.12:c.432+264T>C	ENSP00000308452.8:n.432+264T>C
ENST00000463128.5:c.-184+264T>C	ENSP00000468672.1:n.-184+264T>C
ENST00000491673.1:n.498+264T>C
ENST00000493253.5:n.219+264T>C
ENST00000540235.5:c.183+264T>C	ENSP00000441751.2:n.183+264T>C
ENST00000577817.3:c.387+264T>C	ENSP00000467418.1:n.387+264T>C
NM_000422.2:c.432+264T>C	NP_000413.1:n.432+264T>C
NM_000422.3:c.432+264T>C MANE Select	NP_000413.1:n.432+264T>C