Canonical Allele Identifier: CA8563254
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs747001866

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612176G>A , CM000679.2:g.41612176G>A GRCh38
NC_000017.10:g.39768428G>A , CM000679.1:g.39768428G>A GRCh37
NC_000017.9:g.37021954G>A NCBI36
NG_008301.1:g.5652C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.513C>T MANE Select ENSP00000301653.3:p.Ile171=
ENST00000301653.8:c.513C>T ENSP00000301653.3:p.Ile171=
ENST00000588319.1:n.590C>T
ENST00000593067.1:c.-202C>T ENSP00000467124.1:n.-202C>T
NM_005557.3:c.513C>T NP_005548.2:p.Ile171=
NM_005557.4:c.513C>T MANE Select NP_005548.2:p.Ile171=