Canonical Allele Identifier: CA480069814
Gene: KRT6A HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52886457G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492673G>A , CM000674.2:g.52492673G>A GRCh38
NC_000012.11:g.52886457G>A , CM000674.1:g.52886457G>A GRCh37
NC_000012.10:g.51172724G>A NCBI36
NG_008298.1:g.5725C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.516C>T MANE Select ENSP00000369317.3:p.Asn172=
ENST00000330722.6:c.516C>T ENSP00000369317.3:p.Asn172=
ENST00000549898.5:n.37C>T
NM_005554.3:c.516C>T NP_005545.1:p.Asn172=
NM_005554.4:c.516C>T MANE Select NP_005545.1:p.Asn172=