Canonical Allele Identifier: CA384952751
Gene: KRT6A HGNC NCBI

Linked Data

COSMIC: COSM6137381
MyVariant Identifiers: chr12:g.52881659T>A (hg19) chr12:g.52487875T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487875T>A , CM000674.2:g.52487875T>A GRCh38
NC_000012.11:g.52881659T>A , CM000674.1:g.52881659T>A GRCh37
NC_000012.10:g.51167926T>A NCBI36
NG_008298.1:g.10523A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1540A>T MANE Select ENSP00000369317.3:p.Ser514Cys
ENST00000330722.6:c.1540A>T ENSP00000369317.3:p.Ser514Cys
NM_005554.3:c.1540A>T NP_005545.1:p.Ser514Cys
NM_005554.4:c.1540A>T MANE Select NP_005545.1:p.Ser514Cys
Search 100 bp 5'
Search 100 bp 3'