Canonical Allele Identifier: CA1307543717

Gene: SLC25A12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171855834C= , CM000664.2:g.171855834C=	GRCh38
NC_000002.11:g.172712344C= , CM000664.1:g.172712344C=	GRCh37
NC_000002.10:g.172420590C=	NCBI36
NG_011781.1:g.43470G=
NG_011781.2:g.43470G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.325G= MANE Select	ENSP00000388658.2:p.Glu109=
ENST00000263812.8:c.210-11326G=	ENSP00000263812.4:n.210-11326G=
ENST00000422440.6:c.325G=	ENSP00000388658.2:p.Glu109=
ENST00000426896.5:c.325G=	ENSP00000413968.1:p.Gly109=
ENST00000472748.5:n.490G=
ENST00000475360.6:c.313G=	ENSP00000437845.1:p.Gly105=
ENST00000484227.5:n.523G=
NM_003705.4:c.325G=	NP_003696.2:p.Glu109=
NR_047549.1:n.302-11326G=
XM_005246923.3:c.274G=	XP_005246980.1:p.Glu92=
XM_011512069.1:c.325G=	XP_011510371.1:p.Glu109=
XM_011512070.1:c.-53G=	XP_011510372.1:n.-53G=
XM_011512070.3:c.-53G=	XP_011510372.1:n.-53G=
NM_003705.5:c.325G= MANE Select	NP_003696.2:p.Glu109=
NR_047549.2:n.240-11326G=