Canonical Allele Identifier: CA480069654
Gene: KRT5 HGNC NCBI

Linked Data

dbSNP Id: rs1420615414
gnomAD v2: 12-52910479-G-A
gnomAD v4: 12-52516695-G-A
MyVariant Identifiers: chr12:g.52910479G>A (hg19) chr12:g.52516695G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516695G>A , CM000674.2:g.52516695G>A GRCh38
NC_000012.11:g.52910479G>A , CM000674.1:g.52910479G>A GRCh37
NC_000012.10:g.51196746G>A NCBI36
NG_008297.1:g.8765C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1381C>T MANE Select ENSP00000252242.4:p.Leu461=
ENST00000252242.8:c.1381C>T ENSP00000252242.4:p.Leu461=
ENST00000547890.5:n.759C>T
ENST00000548409.5:c.503C>T
ENST00000549511.5:n.588C>T
ENST00000552629.5:n.1479C>T
NM_000424.3:c.1381C>T NP_000415.2:p.Leu461=
NM_000424.4:c.1381C>T MANE Select NP_000415.2:p.Leu461=
Search 100 bp 5'
Search 100 bp 3'