Canonical Allele Identifier: CA2578079202
Gene: GABRA4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46993252A>T , CM000666.2:g.46993252A>T GRCh38
NC_000004.11:g.46995269A>T , CM000666.1:g.46995269A>T GRCh37
NC_000004.10:g.46690026A>T NCBI36
NG_011809.1:g.5312T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264318.4:c.86+87T>A MANE Select ENSP00000264318.3:n.86+87T>A
ENST00000264318.3:c.86+87T>A ENSP00000264318.3:n.86+87T>A
ENST00000502874.1:c.86+87T>A ENSP00000424386.1:n.86+87T>A
ENST00000508560.5:c.18+155T>A ENSP00000425445.1:n.18+155T>A
ENST00000509316.1:n.210+87T>A
ENST00000511523.5:c.18+155T>A ENSP00000422152.1:n.18+155T>A
NM_000809.3:c.86+87T>A NP_000800.2:n.86+87T>A
NM_001204266.1:c.29+155T>A NP_001191195.1:n.29+155T>A
NM_001204267.1:c.29+155T>A NP_001191196.1:n.29+155T>A
XM_011513677.1:c.86+87T>A XP_011511979.1:n.86+87T>A
NM_000809.4:c.86+87T>A MANE Select NP_000800.2:n.86+87T>A
NM_001204266.2:c.29+155T>A NP_001191195.1:n.29+155T>A
NM_001204267.2:c.29+155T>A NP_001191196.1:n.29+155T>A
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