Canonical Allele Identifier: CA500187653
Gene: KRT12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39023397G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867145G>A , CM000679.2:g.40867145G>A GRCh38
NC_000017.10:g.39023397G>A , CM000679.1:g.39023397G>A GRCh37
NC_000017.9:g.36276923G>A NCBI36
NG_008077.1:g.5066C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.42C>T MANE Select ENSP00000251643.4:p.Thr14=
ENST00000647902.1:c.42C>T ENSP00000497770.1:p.Thr14=
ENST00000251643.4:c.42C>T ENSP00000251643.4:p.Thr14=
NM_000223.3:c.42C>T NP_000214.1:p.Thr14=
XR_934754.1:n.1500+16285G>A
XR_934754.2:n.2008+16285G>A
NM_000223.4:c.42C>T MANE Select NP_000214.1:p.Thr14=
Search 100 bp 5'
Search 100 bp 3'