Canonical Allele Identifier: CA384963339
Gene: KRT6A HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52886458T>A (hg19) chr12:g.52492674T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492674T>A , CM000674.2:g.52492674T>A GRCh38
NC_000012.11:g.52886458T>A , CM000674.1:g.52886458T>A GRCh37
NC_000012.10:g.51172725T>A NCBI36
NG_008298.1:g.5724A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.515A>T MANE Select ENSP00000369317.3:p.Asn172Ile
ENST00000330722.6:c.515A>T ENSP00000369317.3:p.Asn172Ile
ENST00000549898.5:n.36A>T
NM_005554.3:c.515A>T NP_005545.1:p.Asn172Ile
NM_005554.4:c.515A>T MANE Select NP_005545.1:p.Asn172Ile
Search 100 bp 5'
Search 100 bp 3'