Canonical Allele Identifier: CA399495310
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs1338121048

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612399C>A , CM000679.2:g.41612399C>A GRCh38
NC_000017.10:g.39768651C>A , CM000679.1:g.39768651C>A GRCh37
NC_000017.9:g.37022177C>A NCBI36
NG_008301.1:g.5429G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.290G>T MANE Select ENSP00000301653.3:p.Gly97Val
ENST00000301653.8:c.290G>T ENSP00000301653.3:p.Gly97Val
ENST00000588319.1:n.367G>T
ENST00000593067.1:c.-312-113G>T ENSP00000467124.1:n.-312-113G>T
NM_005557.3:c.290G>T NP_005548.2:p.Gly97Val
NM_005557.4:c.290G>T MANE Select NP_005548.2:p.Gly97Val