Canonical Allele Identifier: CA500206144

Gene: KRT16

Linked Data

• MyVariant Identifiers: chr17:g.39768665A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612413A>G , CM000679.2:g.41612413A>G	GRCh38
NC_000017.10:g.39768665A>G , CM000679.1:g.39768665A>G	GRCh37
NC_000017.9:g.37022191A>G	NCBI36
NG_008301.1:g.5415T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.276T>C MANE Select	ENSP00000301653.3:p.Ala92=
ENST00000301653.8:c.276T>C	ENSP00000301653.3:p.Ala92=
ENST00000588319.1:n.353T>C
ENST00000593067.1:c.-312-127T>C	ENSP00000467124.1:n.-312-127T>C
NM_005557.3:c.276T>C	NP_005548.2:p.Ala92=
NM_005557.4:c.276T>C MANE Select	NP_005548.2:p.Ala92=