Canonical Allele Identifier: CA500206446
Gene: KRT16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39768470C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612218C>T , CM000679.2:g.41612218C>T GRCh38
NC_000017.10:g.39768470C>T , CM000679.1:g.39768470C>T GRCh37
NC_000017.9:g.37021996C>T NCBI36
NG_008301.1:g.5610G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.471G>A MANE Select ENSP00000301653.3:p.Arg157=
ENST00000301653.8:c.471G>A ENSP00000301653.3:p.Arg157=
ENST00000588319.1:n.548G>A
ENST00000593067.1:c.-244G>A ENSP00000467124.1:n.-244G>A
NM_005557.3:c.471G>A NP_005548.2:p.Arg157=
NM_005557.4:c.471G>A MANE Select NP_005548.2:p.Arg157=