Canonical Allele Identifier: CA6582535
Gene: KRT5 HGNC NCBI

Linked Data

dbSNP Id: rs755117771
ExAC: 12:52910450 G / A
gnomAD v2: 12-52910450-G-A
gnomAD v3: 12-52516666-G-A
gnomAD v4: 12-52516666-G-A
MyVariant Identifiers: chr12:g.52910450G>A (hg19) chr12:g.52516666G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516666G>A , CM000674.2:g.52516666G>A GRCh38
NC_000012.11:g.52910450G>A , CM000674.1:g.52910450G>A GRCh37
NC_000012.10:g.51196717G>A NCBI36
NG_008297.1:g.8794C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1410C>T MANE Select ENSP00000252242.4:p.Tyr470=
ENST00000252242.8:c.1410C>T ENSP00000252242.4:p.Tyr470=
ENST00000548409.5:c.532C>T
ENST00000549511.5:n.617C>T
ENST00000552629.5:n.1508C>T
NM_000424.3:c.1410C>T NP_000415.2:p.Tyr470=
NM_000424.4:c.1410C>T MANE Select NP_000415.2:p.Tyr470=
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