Canonical Allele Identifier: CA2036520082
Gene: KRT6A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487950C= , CM000674.2:g.52487950C= GRCh38
NC_000012.11:g.52881734C= , CM000674.1:g.52881734C= GRCh37
NC_000012.10:g.51168001C= NCBI36
NG_008298.1:g.10448G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1465G= MANE Select ENSP00000369317.3:p.Val489=
ENST00000330722.6:c.1465G= ENSP00000369317.3:p.Val489=
NM_005554.3:c.1465G= NP_005545.1:p.Val489=
NM_005554.4:c.1465G= MANE Select NP_005545.1:p.Val489=
Search 100 bp 5'
Search 100 bp 3'