Canonical Allele Identifier: CA399497492
Gene: KRT16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612675C>A , CM000679.2:g.41612675C>A GRCh38
NC_000017.10:g.39768927C>A , CM000679.1:g.39768927C>A GRCh37
NC_000017.9:g.37022453C>A NCBI36
NG_008301.1:g.5153G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.14G>T MANE Select ENSP00000301653.3:p.Ser5Ile
ENST00000301653.8:c.14G>T ENSP00000301653.3:p.Ser5Ile
ENST00000588319.1:n.91G>T
ENST00000590990.1:c.14G>T ENSP00000467105.1:p.Ser5Ile
ENST00000593067.1:c.-313+115G>T ENSP00000467124.1:n.-313+115G>T
NM_005557.3:c.14G>T NP_005548.2:p.Ser5Ile
NM_005557.4:c.14G>T MANE Select NP_005548.2:p.Ser5Ile