Canonical Allele Identifier: CA500187578
Gene: KRT12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39023346C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867094C>T , CM000679.2:g.40867094C>T GRCh38
NC_000017.10:g.39023346C>T , CM000679.1:g.39023346C>T GRCh37
NC_000017.9:g.36276872C>T NCBI36
NG_008077.1:g.5117G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.93G>A MANE Select ENSP00000251643.4:p.Arg31=
ENST00000647902.1:c.93G>A ENSP00000497770.1:p.Arg31=
ENST00000251643.4:c.93G>A ENSP00000251643.4:p.Arg31=
NM_000223.3:c.93G>A NP_000214.1:p.Arg31=
XR_934754.1:n.1500+16234C>T
XR_934754.2:n.2008+16234C>T
NM_000223.4:c.93G>A MANE Select NP_000214.1:p.Arg31=