Canonical Allele Identifier: CA358896489

Gene: SLC25A4

Linked Data

• MyVariant Identifiers: chr4:g.186066182A>T (hg19) ; chr4:g.185145028A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.185145028A>T , CM000666.2:g.185145028A>T	GRCh38
NC_000004.11:g.186066182A>T , CM000666.1:g.186066182A>T	GRCh37
NC_000004.10:g.186303176A>T	NCBI36
NG_013001.1:g.6766A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281456.11:c.376A>T MANE Select	ENSP00000281456.5:p.Thr126Ser
ENST00000281456.10:c.376A>T	ENSP00000281456.5:p.Thr126Ser
ENST00000491736.1:c.376A>T	ENSP00000476711.1:p.Thr126Ser
NM_001151.3:c.376A>T	NP_001142.2:p.Thr126Ser
NM_001151.4:c.376A>T MANE Select	NP_001142.2:p.Thr126Ser