Canonical Allele Identifier: CA500187145
Gene: KRT12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39022968A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866716A>T , CM000679.2:g.40866716A>T GRCh38
NC_000017.10:g.39022968A>T , CM000679.1:g.39022968A>T GRCh37
NC_000017.9:g.36276494A>T NCBI36
NG_008077.1:g.5495T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.471T>A MANE Select ENSP00000251643.4:p.Ile157=
ENST00000647902.1:c.363T>A ENSP00000497770.1:p.Ile121=
ENST00000251643.4:c.471T>A ENSP00000251643.4:p.Ile157=
NM_000223.3:c.471T>A NP_000214.1:p.Ile157=
XR_934754.1:n.1500+15856A>T
XR_934754.2:n.2008+15856A>T
NM_000223.4:c.471T>A MANE Select NP_000214.1:p.Ile157=
Search 100 bp 5'
Search 100 bp 3'