Canonical Allele Identifier: CA399494562
Gene: KRT16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612268C>T , CM000679.2:g.41612268C>T GRCh38
NC_000017.10:g.39768520C>T , CM000679.1:g.39768520C>T GRCh37
NC_000017.9:g.37022046C>T NCBI36
NG_008301.1:g.5560G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.421G>A MANE Select ENSP00000301653.3:p.Ala141Thr
ENST00000301653.8:c.421G>A ENSP00000301653.3:p.Ala141Thr
ENST00000588319.1:n.498G>A
ENST00000593067.1:c.-294G>A ENSP00000467124.1:n.-294G>A
NM_005557.3:c.421G>A NP_005548.2:p.Ala141Thr
NM_005557.4:c.421G>A MANE Select NP_005548.2:p.Ala141Thr