Canonical Allele Identifier: CA290686146

Gene: KRT17

Linked Data

• dbSNP Id: rs953768141
• gnomAD v4: 17-41624279-A-G
• MyVariant Identifiers: chr17:g.39780531A>G (hg19) ; chr17:g.41624279A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624279A>G , CM000679.2:g.41624279A>G	GRCh38
NC_000017.10:g.39780531A>G , CM000679.1:g.39780531A>G	GRCh37
NC_000017.9:g.37034057A>G	NCBI36
NG_008625.1:g.5352T>C
NG_009090.2:g.167434T>C , LRG_401:g.167434T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.231T>C MANE Select	ENSP00000308452.8:p.Asp77=
ENST00000311208.12:c.231T>C	ENSP00000308452.8:p.Asp77=
ENST00000463128.5:c.-312-73T>C	ENSP00000468672.1:n.-312-73T>C
ENST00000491673.1:n.297T>C
ENST00000493253.5:n.18T>C
ENST00000540235.5:c.26T>C	ENSP00000441751.2:p.Met9Thr
ENST00000577817.3:c.186T>C	ENSP00000467418.1:p.Asp62=
NM_000422.2:c.231T>C	NP_000413.1:p.Asp77=
NM_000422.3:c.231T>C MANE Select	NP_000413.1:p.Asp77=