Canonical Allele Identifier: CA2260099649
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612230G= , CM000679.2:g.41612230G= GRCh38
NC_000017.10:g.39768482G= , CM000679.1:g.39768482G= GRCh37
NC_000017.9:g.37022008G= NCBI36
NG_008301.1:g.5598C=

Transcript Alleles

HGVS Amino-acid change
ENST00000301653.9:c.459C= MANE Select ENSP00000301653.3:p.Tyr153=
ENST00000301653.8:c.459C= ENSP00000301653.3:p.Tyr153=
ENST00000588319.1:n.536C=
ENST00000593067.1:c.-256C= ENSP00000467124.1:n.-256C=
NM_005557.3:c.459C= NP_005548.2:p.Tyr153=
NM_005557.4:c.459C= MANE Select NP_005548.2:p.Tyr153=