Canonical Allele Identifier: CA2618927907
Gene: KRT6A HGNC NCBI

Linked Data

gnomAD v4: 12-52487995-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487995G>A , CM000674.2:g.52487995G>A GRCh38
NC_000012.11:g.52881779G>A , CM000674.1:g.52881779G>A GRCh37
NC_000012.10:g.51168046G>A NCBI36
NG_008298.1:g.10403C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1460-40C>T MANE Select ENSP00000369317.3:n.1460-40C>T
ENST00000330722.6:c.1460-40C>T ENSP00000369317.3:n.1460-40C>T
NM_005554.3:c.1460-40C>T NP_005545.1:n.1460-40C>T
NM_005554.4:c.1460-40C>T MANE Select NP_005545.1:n.1460-40C>T
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