Canonical Allele Identifier: CA2260099798
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612497C= , CM000679.2:g.41612497C= GRCh38
NC_000017.10:g.39768749C= , CM000679.1:g.39768749C= GRCh37
NC_000017.9:g.37022275C= NCBI36
NG_008301.1:g.5331G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.192G= MANE Select ENSP00000301653.3:p.Leu64=
ENST00000301653.8:c.192G= ENSP00000301653.3:p.Leu64=
ENST00000588319.1:n.269G=
ENST00000593067.1:c.-312-211G= ENSP00000467124.1:n.-312-211G=
NM_005557.3:c.192G= NP_005548.2:p.Leu64=
NM_005557.4:c.192G= MANE Select NP_005548.2:p.Leu64=