Canonical Allele Identifier: CA500187579
Gene: KRT12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39023348T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867096T>G , CM000679.2:g.40867096T>G GRCh38
NC_000017.10:g.39023348T>G , CM000679.1:g.39023348T>G GRCh37
NC_000017.9:g.36276874T>G NCBI36
NG_008077.1:g.5115A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.91A>C MANE Select ENSP00000251643.4:p.Arg31=
ENST00000647902.1:c.91A>C ENSP00000497770.1:p.Arg31=
ENST00000251643.4:c.91A>C ENSP00000251643.4:p.Arg31=
NM_000223.3:c.91A>C NP_000214.1:p.Arg31=
XR_934754.1:n.1500+16236T>G
XR_934754.2:n.2008+16236T>G
NM_000223.4:c.91A>C MANE Select NP_000214.1:p.Arg31=
Search 100 bp 5'
Search 100 bp 3'