Canonical Allele Identifier: CA399389212
Gene: KRT12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866997C>G , CM000679.2:g.40866997C>G GRCh38
NC_000017.10:g.39023249C>G , CM000679.1:g.39023249C>G GRCh37
NC_000017.9:g.36276775C>G NCBI36
NG_008077.1:g.5214G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.190G>C MANE Select ENSP00000251643.4:p.Gly64Arg
ENST00000647902.1:c.190G>C ENSP00000497770.1:p.Gly64Arg
ENST00000251643.4:c.190G>C ENSP00000251643.4:p.Gly64Arg
NM_000223.3:c.190G>C NP_000214.1:p.Gly64Arg
XR_934754.1:n.1500+16137C>G
XR_934754.2:n.2008+16137C>G
NM_000223.4:c.190G>C MANE Select NP_000214.1:p.Gly64Arg