Canonical Allele Identifier: CA399494238

Gene: KRT16

Linked Data

• MyVariant Identifiers: chr17:g.39768461C>A (hg19) ; chr17:g.41612209C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612209C>A , CM000679.2:g.41612209C>A	GRCh38
NC_000017.10:g.39768461C>A , CM000679.1:g.39768461C>A	GRCh37
NC_000017.9:g.37021987C>A	NCBI36
NG_008301.1:g.5619G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.480G>T MANE Select	ENSP00000301653.3:p.Glu160Asp
ENST00000301653.8:c.480G>T	ENSP00000301653.3:p.Glu160Asp
ENST00000588319.1:n.557G>T
ENST00000593067.1:c.-235G>T	ENSP00000467124.1:n.-235G>T
NM_005557.3:c.480G>T	NP_005548.2:p.Glu160Asp
NM_005557.4:c.480G>T MANE Select	NP_005548.2:p.Glu160Asp