Canonical Allele Identifier: CA389465307

Gene: SLC25A21

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.36684834T>C , CM000676.2:g.36684834T>C	GRCh38
NC_000014.8:g.37154039T>C , CM000676.1:g.37154039T>C	GRCh37
NC_000014.7:g.36223790T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_030631.4:c.695A>G MANE Select	NP_085134.1:p.Lys232Arg
ENST00000331299.6:c.695A>G MANE Select	ENSP00000329452.5:p.Lys232Arg
NM_001171170.1:c.695A>G	NP_001164641.1:p.Lys232Arg
NM_001171170.2:c.695A>G	NP_001164641.1:p.Lys232Arg
NM_030631.3:c.695A>G	NP_085134.1:p.Lys232Arg
ENST00000331299.5:c.695A>G	ENSP00000329452.5:p.Lys232Arg
ENST00000555449.5:c.695A>G	ENSP00000451873.1:p.Lys232Arg
ENST00000622765.4:c.500A>G	ENSP00000481445.1:p.Lys167Arg
XM_011537287.1:c.707A>G	XP_011535589.1:p.Lys236Arg
XM_011537287.3:c.707A>G	XP_011535589.1:p.Lys236Arg
XM_011537288.1:c.605A>G	XP_011535590.1:p.Lys202Arg
XM_011537288.3:c.605A>G	XP_011535590.1:p.Lys202Arg
XM_011537289.1:c.599A>G	XP_011535591.1:p.Lys200Arg
XM_011537289.3:c.599A>G	XP_011535591.1:p.Lys200Arg