Canonical Allele Identifier: CA2260099708
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612334C= , CM000679.2:g.41612334C= GRCh38
NC_000017.10:g.39768586C= , CM000679.1:g.39768586C= GRCh37
NC_000017.9:g.37022112C= NCBI36
NG_008301.1:g.5494G=

Transcript Alleles

HGVS Amino-acid change
ENST00000301653.9:c.355G= MANE Select ENSP00000301653.3:p.Val119=
ENST00000301653.8:c.355G= ENSP00000301653.3:p.Val119=
ENST00000588319.1:n.432G=
ENST00000593067.1:c.-312-48G= ENSP00000467124.1:n.-312-48G=
NM_005557.3:c.355G= NP_005548.2:p.Val119=
NM_005557.4:c.355G= MANE Select NP_005548.2:p.Val119=