Canonical Allele Identifier: CA2260099648
Gene: KRT16 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000301653.9:c.460C= MANE Select ENSP00000301653.3:p.Gln154=
ENST00000301653.8:c.460C= ENSP00000301653.3:p.Gln154=
ENST00000588319.1:n.537C=
ENST00000593067.1:c.-255C= ENSP00000467124.1:n.-255C=
NM_005557.3:c.460C= NP_005548.2:p.Gln154=
NM_005557.4:c.460C= MANE Select NP_005548.2:p.Gln154=