Canonical Allele Identifier: CA358896097

Gene: SLC25A4

Linked Data

• MyVariant Identifiers: chr4:g.186066003G>T (hg19) ; chr4:g.185144849G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.185144849G>T , CM000666.2:g.185144849G>T	GRCh38
NC_000004.11:g.186066003G>T , CM000666.1:g.186066003G>T	GRCh37
NC_000004.10:g.186302997G>T	NCBI36
NG_013001.1:g.6587G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281456.11:c.197G>T MANE Select	ENSP00000281456.5:p.Gly66Val
ENST00000281456.10:c.197G>T	ENSP00000281456.5:p.Gly66Val
ENST00000491736.1:c.197G>T	ENSP00000476711.1:p.Gly66Val
NM_001151.3:c.197G>T	NP_001142.2:p.Gly66Val
NM_001151.4:c.197G>T MANE Select	NP_001142.2:p.Gly66Val