Canonical Allele Identifier: CA2637841008

Gene: KRT17

Linked Data

• gnomAD v4: 17-41624558-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624558A>C , CM000679.2:g.41624558A>C	GRCh38
NC_000017.10:g.39780810A>C , CM000679.1:g.39780810A>C	GRCh37
NC_000017.9:g.37034336A>C	NCBI36
NG_008625.1:g.5073T>G
NG_009090.2:g.167155T>G , LRG_401:g.167155T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.-49T>G MANE Select	ENSP00000308452.8:n.-49T>G
ENST00000311208.12:c.-49T>G	ENSP00000308452.8:n.-49T>G
ENST00000463128.5:c.-313+185T>G	ENSP00000468672.1:n.-313+185T>G
ENST00000491673.1:n.18T>G
NM_000422.2:c.-49T>G	NP_000413.1:n.-49T>G
NM_000422.3:c.-49T>G MANE Select	NP_000413.1:n.-49T>G