Canonical Allele Identifier: CA772031473

Gene: KRT17

Linked Data

• dbSNP Id: rs1397496446
• gnomAD v3: 17-41623756-G-A
• gnomAD v4: 17-41623756-G-A
• MyVariant Identifiers: chr17:g.39780008G>A (hg19) ; chr17:g.41623756G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41623756G>A , CM000679.2:g.41623756G>A	GRCh38
NC_000017.10:g.39780008G>A , CM000679.1:g.39780008G>A	GRCh37
NC_000017.9:g.37033534G>A	NCBI36
NG_008625.1:g.5875C>T
NG_009090.2:g.167957C>T , LRG_401:g.167957C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.432+322C>T MANE Select	ENSP00000308452.8:n.432+322C>T
ENST00000311208.12:c.432+322C>T	ENSP00000308452.8:n.432+322C>T
ENST00000463128.5:c.-184+322C>T	ENSP00000468672.1:n.-184+322C>T
ENST00000491673.1:n.498+322C>T
ENST00000493253.5:n.219+322C>T
ENST00000540235.5:c.183+322C>T	ENSP00000441751.2:n.183+322C>T
ENST00000577817.3:c.387+322C>T	ENSP00000467418.1:n.387+322C>T
NM_000422.2:c.432+322C>T	NP_000413.1:n.432+322C>T
NM_000422.3:c.432+322C>T MANE Select	NP_000413.1:n.432+322C>T