Canonical Allele Identifier: CA2637840812

Gene: KRT17

Linked Data

• gnomAD v4: 17-41623941-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41623941T>C , CM000679.2:g.41623941T>C	GRCh38
NC_000017.10:g.39780193T>C , CM000679.1:g.39780193T>C	GRCh37
NC_000017.9:g.37033719T>C	NCBI36
NG_008625.1:g.5690A>G
NG_009090.2:g.167772A>G , LRG_401:g.167772A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.432+137A>G MANE Select	ENSP00000308452.8:n.432+137A>G
ENST00000311208.12:c.432+137A>G	ENSP00000308452.8:n.432+137A>G
ENST00000463128.5:c.-184+137A>G	ENSP00000468672.1:n.-184+137A>G
ENST00000491673.1:n.498+137A>G
ENST00000493253.5:n.219+137A>G
ENST00000540235.5:c.183+137A>G	ENSP00000441751.2:n.183+137A>G
ENST00000577817.3:c.387+137A>G	ENSP00000467418.1:n.387+137A>G
NM_000422.2:c.432+137A>G	NP_000413.1:n.432+137A>G
NM_000422.3:c.432+137A>G MANE Select	NP_000413.1:n.432+137A>G