Canonical Allele Identifier: CA442614670
Gene: SLC25A4 HGNC NCBI

Linked Data

gnomAD v4: 4-185143411-G-A
MyVariant Identifiers: chr4:g.186064565G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185143411G>A , CM000666.2:g.185143411G>A GRCh38
NC_000004.11:g.186064565G>A , CM000666.1:g.186064565G>A GRCh37
NC_000004.10:g.186301559G>A NCBI36
NG_013001.1:g.5149G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.39G>A MANE Select ENSP00000281456.5:p.Leu13=
ENST00000281456.10:c.39G>A ENSP00000281456.5:p.Leu13=
ENST00000491736.1:c.39G>A ENSP00000476711.1:p.Leu13=
NM_001151.3:c.39G>A NP_001142.2:p.Leu13=
NM_001151.4:c.39G>A MANE Select NP_001142.2:p.Leu13=
Search 100 bp 5'
Search 100 bp 3'