Canonical Allele Identifier: CA500206099

Gene: KRT16

Linked Data

• MyVariant Identifiers: chr17:g.39768641A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612389A>T , CM000679.2:g.41612389A>T	GRCh38
NC_000017.10:g.39768641A>T , CM000679.1:g.39768641A>T	GRCh37
NC_000017.9:g.37022167A>T	NCBI36
NG_008301.1:g.5439T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.300T>A MANE Select	ENSP00000301653.3:p.Ala100=
ENST00000301653.8:c.300T>A	ENSP00000301653.3:p.Ala100=
ENST00000588319.1:n.377T>A
ENST00000593067.1:c.-312-103T>A	ENSP00000467124.1:n.-312-103T>A
NM_005557.3:c.300T>A	NP_005548.2:p.Ala100=
NM_005557.4:c.300T>A MANE Select	NP_005548.2:p.Ala100=