Canonical Allele Identifier: CA399389217
Gene: KRT12 HGNC NCBI

Linked Data

dbSNP Id: rs1597844328

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866998A>T , CM000679.2:g.40866998A>T GRCh38
NC_000017.10:g.39023250A>T , CM000679.1:g.39023250A>T GRCh37
NC_000017.9:g.36276776A>T NCBI36
NG_008077.1:g.5213T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.189T>A MANE Select ENSP00000251643.4:p.Phe63Leu
ENST00000647902.1:c.189T>A ENSP00000497770.1:p.Phe63Leu
ENST00000251643.4:c.189T>A ENSP00000251643.4:p.Phe63Leu
NM_000223.3:c.189T>A NP_000214.1:p.Phe63Leu
XR_934754.1:n.1500+16138A>T
XR_934754.2:n.2008+16138A>T
NM_000223.4:c.189T>A MANE Select NP_000214.1:p.Phe63Leu