Canonical Allele Identifier: CA2259745894
Gene: KRT12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866957A= , CM000679.2:g.40866957A= GRCh38
NC_000017.10:g.39023209A= , CM000679.1:g.39023209A= GRCh37
NC_000017.9:g.36276735A= NCBI36
NG_008077.1:g.5254T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.230T= MANE Select ENSP00000251643.4:p.Met77=
ENST00000647902.1:c.211+19T= ENSP00000497770.1:n.211+19T=
ENST00000251643.4:c.230T= ENSP00000251643.4:p.Met77=
NM_000223.3:c.230T= NP_000214.1:p.Met77=
XR_934754.1:n.1500+16097A=
XR_934754.2:n.2008+16097A=
NM_000223.4:c.230T= MANE Select NP_000214.1:p.Met77=