Canonical Allele Identifier: CA399389144
Gene: KRT12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39023232A>T (hg19) chr17:g.40866980A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866980A>T , CM000679.2:g.40866980A>T GRCh38
NC_000017.10:g.39023232A>T , CM000679.1:g.39023232A>T GRCh37
NC_000017.9:g.36276758A>T NCBI36
NG_008077.1:g.5231T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.207T>A MANE Select ENSP00000251643.4:p.Phe69Leu
ENST00000647902.1:c.207T>A ENSP00000497770.1:p.Phe69Leu
ENST00000251643.4:c.207T>A ENSP00000251643.4:p.Phe69Leu
NM_000223.3:c.207T>A NP_000214.1:p.Phe69Leu
XR_934754.1:n.1500+16120A>T
XR_934754.2:n.2008+16120A>T
NM_000223.4:c.207T>A MANE Select NP_000214.1:p.Phe69Leu
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