Canonical Allele Identifier: CA399494351
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs1908224972

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612229G>A , CM000679.2:g.41612229G>A GRCh38
NC_000017.10:g.39768481G>A , CM000679.1:g.39768481G>A GRCh37
NC_000017.9:g.37022007G>A NCBI36
NG_008301.1:g.5599C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000301653.9:c.460C>T MANE Select ENSP00000301653.3:p.Gln154Ter
ENST00000301653.8:c.460C>T ENSP00000301653.3:p.Gln154Ter
ENST00000588319.1:n.537C>T
ENST00000593067.1:c.-255C>T ENSP00000467124.1:n.-255C>T
NM_005557.3:c.460C>T NP_005548.2:p.Gln154Ter
NM_005557.4:c.460C>T MANE Select NP_005548.2:p.Gln154Ter