Canonical Allele Identifier: CA2809496591

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612108C>A , CM000679.2:g.41612108C>A	GRCh38
NC_000017.10:g.39768360C>A , CM000679.1:g.39768360C>A	GRCh37
NC_000017.9:g.37021886C>A	NCBI36
NG_008301.1:g.5720G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.531+50G>T MANE Select	ENSP00000301653.3:n.531+50G>T
ENST00000301653.8:c.531+50G>T	ENSP00000301653.3:n.531+50G>T
ENST00000588319.1:n.658G>T
ENST00000593067.1:c.-184+50G>T	ENSP00000467124.1:n.-184+50G>T
NM_005557.3:c.531+50G>T	NP_005548.2:n.531+50G>T
NM_005557.4:c.531+50G>T MANE Select	NP_005548.2:n.531+50G>T