Canonical Allele Identifier: CA500187515
Gene: KRT12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39023316A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867064A>G , CM000679.2:g.40867064A>G GRCh38
NC_000017.10:g.39023316A>G , CM000679.1:g.39023316A>G GRCh37
NC_000017.9:g.36276842A>G NCBI36
NG_008077.1:g.5147T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.123T>C MANE Select ENSP00000251643.4:p.Gly41=
ENST00000647902.1:c.123T>C ENSP00000497770.1:p.Gly41=
ENST00000251643.4:c.123T>C ENSP00000251643.4:p.Gly41=
NM_000223.3:c.123T>C NP_000214.1:p.Gly41=
XR_934754.1:n.1500+16204A>G
XR_934754.2:n.2008+16204A>G
NM_000223.4:c.123T>C MANE Select NP_000214.1:p.Gly41=