Canonical Allele Identifier: CA1519345452
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1734377829
gnomAD v4: 4-185143339-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185143339G>A , CM000666.2:g.185143339G>A GRCh38
NC_000004.11:g.186064493G>A , CM000666.1:g.186064493G>A GRCh37
NC_000004.10:g.186301487G>A NCBI36
NG_013001.1:g.5077G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.-34G>A MANE Select ENSP00000281456.5:n.-34G>A
ENST00000281456.10:c.-34G>A ENSP00000281456.5:n.-34G>A
ENST00000491736.1:c.-34G>A ENSP00000476711.1:n.-34G>A
NM_001151.3:c.-34G>A NP_001142.2:n.-34G>A
NM_001151.4:c.-34G>A MANE Select NP_001142.2:n.-34G>A
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