Canonical Allele Identifier: CA8563265
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs751241027

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612224C>T , CM000679.2:g.41612224C>T GRCh38
NC_000017.10:g.39768476C>T , CM000679.1:g.39768476C>T GRCh37
NC_000017.9:g.37022002C>T NCBI36
NG_008301.1:g.5604G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301653.9:c.465G>A MANE Select ENSP00000301653.3:p.Arg155=
ENST00000301653.8:c.465G>A ENSP00000301653.3:p.Arg155=
ENST00000588319.1:n.542G>A
ENST00000593067.1:c.-250G>A ENSP00000467124.1:n.-250G>A
NM_005557.3:c.465G>A NP_005548.2:p.Arg155=
NM_005557.4:c.465G>A MANE Select NP_005548.2:p.Arg155=