Canonical Allele Identifier: CA399512891

Gene: KRT17

Linked Data

• dbSNP Id: rs1196700871
• gnomAD v2: 17-39780548-T-C
• gnomAD v4: 17-41624296-T-C
• MyVariant Identifiers: chr17:g.39780548T>C (hg19) ; chr17:g.41624296T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624296T>C , CM000679.2:g.41624296T>C	GRCh38
NC_000017.10:g.39780548T>C , CM000679.1:g.39780548T>C	GRCh37
NC_000017.9:g.37034074T>C	NCBI36
NG_008625.1:g.5335A>G
NG_009090.2:g.167417A>G , LRG_401:g.167417A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.214A>G MANE Select	ENSP00000308452.8:p.Ser72Gly
ENST00000311208.12:c.214A>G	ENSP00000308452.8:p.Ser72Gly
ENST00000463128.5:c.-312-90A>G	ENSP00000468672.1:n.-312-90A>G
ENST00000491673.1:n.280A>G
ENST00000493253.5:n.1A>G
ENST00000540235.5:c.9A>G	ENSP00000441751.2:p.Ala3=
ENST00000577817.3:c.169A>G	ENSP00000467418.1:p.Ser57Gly
NM_000422.2:c.214A>G	NP_000413.1:p.Ser72Gly
NM_000422.3:c.214A>G MANE Select	NP_000413.1:p.Ser72Gly