Canonical Allele Identifier: CA1307525236

Gene: SLC25A12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171813452C= , CM000664.2:g.171813452C=	GRCh38
NC_000002.11:g.172669962C= , CM000664.1:g.172669962C=	GRCh37
NC_000002.10:g.172378208C=	NCBI36
NG_011781.1:g.85852G=
NG_011781.2:g.85852G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.1058G= MANE Select	ENSP00000388658.2:p.Arg353=
ENST00000263812.8:c.*678G=	ENSP00000263812.4:n.*678G=
ENST00000422440.6:c.1058G=	ENSP00000388658.2:p.Arg353=
NM_003705.4:c.1058G=	NP_003696.2:p.Arg353=
NR_047549.1:n.1034G=
XM_005246923.3:c.1007G=	XP_005246980.1:p.Arg336=
XM_011512069.1:c.1058G=	XP_011510371.1:p.Arg353=
XM_011512070.1:c.785G=	XP_011510372.1:p.Arg262=
XM_011512070.3:c.785G=	XP_011510372.1:p.Arg262=
NM_003705.5:c.1058G= MANE Select	NP_003696.2:p.Arg353=
NR_047549.2:n.972G=