Canonical Allele Identifier: CA399494058
Gene: KRT16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612177A>T , CM000679.2:g.41612177A>T GRCh38
NC_000017.10:g.39768429A>T , CM000679.1:g.39768429A>T GRCh37
NC_000017.9:g.37021955A>T NCBI36
NG_008301.1:g.5651T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.512T>A MANE Select ENSP00000301653.3:p.Ile171Asn
ENST00000301653.8:c.512T>A ENSP00000301653.3:p.Ile171Asn
ENST00000588319.1:n.589T>A
ENST00000593067.1:c.-203T>A ENSP00000467124.1:n.-203T>A
NM_005557.3:c.512T>A NP_005548.2:p.Ile171Asn
NM_005557.4:c.512T>A MANE Select NP_005548.2:p.Ile171Asn