Canonical Allele Identifier: CA399495058

Gene: KRT16

Linked Data

• MyVariant Identifiers: chr17:g.39768613C>A (hg19) ; chr17:g.41612361C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612361C>A , CM000679.2:g.41612361C>A	GRCh38
NC_000017.10:g.39768613C>A , CM000679.1:g.39768613C>A	GRCh37
NC_000017.9:g.37022139C>A	NCBI36
NG_008301.1:g.5467G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.328G>T MANE Select	ENSP00000301653.3:p.Asp110Tyr
ENST00000301653.8:c.328G>T	ENSP00000301653.3:p.Asp110Tyr
ENST00000588319.1:n.405G>T
ENST00000593067.1:c.-312-75G>T	ENSP00000467124.1:n.-312-75G>T
NM_005557.3:c.328G>T	NP_005548.2:p.Asp110Tyr
NM_005557.4:c.328G>T MANE Select	NP_005548.2:p.Asp110Tyr