Canonical Allele Identifier: CA399494684

Gene: KRT16

Linked Data

• MyVariant Identifiers: chr17:g.39768542G>T (hg19) ; chr17:g.41612290G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612290G>T , CM000679.2:g.41612290G>T	GRCh38
NC_000017.10:g.39768542G>T , CM000679.1:g.39768542G>T	GRCh37
NC_000017.9:g.37022068G>T	NCBI36
NG_008301.1:g.5538C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.399C>A MANE Select	ENSP00000301653.3:p.Asp133Glu
ENST00000301653.8:c.399C>A	ENSP00000301653.3:p.Asp133Glu
ENST00000588319.1:n.476C>A
ENST00000593067.1:c.-312-4C>A	ENSP00000467124.1:n.-312-4C>A
NM_005557.3:c.399C>A	NP_005548.2:p.Asp133Glu
NM_005557.4:c.399C>A MANE Select	NP_005548.2:p.Asp133Glu