Canonical Allele Identifier: CA7159264

Gene: SLC25A21

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.36711389G>A , CM000676.2:g.36711389G>A	GRCh38
NC_000014.8:g.37180594G>A , CM000676.1:g.37180594G>A	GRCh37
NC_000014.7:g.36250345G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_030631.4:c.532C>T MANE Select	NP_085134.1:p.Arg178Ter
ENST00000331299.6:c.532C>T MANE Select	ENSP00000329452.5:p.Arg178Ter
NM_001171170.1:c.532C>T	NP_001164641.1:p.Arg178Ter
NM_001171170.2:c.532C>T	NP_001164641.1:p.Arg178Ter
NM_030631.3:c.532C>T	NP_085134.1:p.Arg178Ter
ENST00000331299.5:c.532C>T	ENSP00000329452.5:p.Arg178Ter
ENST00000555449.5:c.532C>T	ENSP00000451873.1:p.Arg178Ter
ENST00000556444.1:n.204C>T
ENST00000622765.4:c.337C>T	ENSP00000481445.1:p.Arg113Ter
XM_011537287.1:c.544C>T	XP_011535589.1:p.Arg182Ter
XM_011537287.3:c.544C>T	XP_011535589.1:p.Arg182Ter
XM_011537288.1:c.442C>T	XP_011535590.1:p.Arg148Ter
XM_011537288.3:c.442C>T	XP_011535590.1:p.Arg148Ter
XM_011537289.1:c.436C>T	XP_011535591.1:p.Arg146Ter
XM_011537289.3:c.436C>T	XP_011535591.1:p.Arg146Ter