Canonical Allele Identifier: CA399494842
Gene: KRT16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612321T>A , CM000679.2:g.41612321T>A GRCh38
NC_000017.10:g.39768573T>A , CM000679.1:g.39768573T>A GRCh37
NC_000017.9:g.37022099T>A NCBI36
NG_008301.1:g.5507A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000301653.9:c.368A>T MANE Select ENSP00000301653.3:p.Asn123Ile
ENST00000301653.8:c.368A>T ENSP00000301653.3:p.Asn123Ile
ENST00000588319.1:n.445A>T
ENST00000593067.1:c.-312-35A>T ENSP00000467124.1:n.-312-35A>T
NM_005557.3:c.368A>T NP_005548.2:p.Asn123Ile
NM_005557.4:c.368A>T MANE Select NP_005548.2:p.Asn123Ile