Canonical Allele Identifier: CA1519346790

Gene: SLC25A4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.185144631T= , CM000666.2:g.185144631T=	GRCh38
NC_000004.11:g.186065785T= , CM000666.1:g.186065785T=	GRCh37
NC_000004.10:g.186302779T=	NCBI36
NG_013001.1:g.6369T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281456.11:c.112-133T= MANE Select	ENSP00000281456.5:n.112-133T=
ENST00000281456.10:c.112-133T=	ENSP00000281456.5:n.112-133T=
ENST00000491736.1:c.112-133T=	ENSP00000476711.1:n.112-133T=
NM_001151.3:c.112-133T=	NP_001142.2:n.112-133T=
NM_001151.4:c.112-133T= MANE Select	NP_001142.2:n.112-133T=