Canonical Allele Identifier: CA1307543692

Gene: SLC25A12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171855777A= , CM000664.2:g.171855777A=	GRCh38
NC_000002.11:g.172712287A= , CM000664.1:g.172712287A=	GRCh37
NC_000002.10:g.172420533A=	NCBI36
NG_011781.1:g.43527T=
NG_011781.2:g.43527T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.325+57T= MANE Select	ENSP00000388658.2:n.325+57T=
ENST00000263812.8:c.210-11269T=	ENSP00000263812.4:n.210-11269T=
ENST00000422440.6:c.325+57T=	ENSP00000388658.2:n.325+57T=
ENST00000426896.5:c.325+57T=	ENSP00000413968.1:n.325+57T=
ENST00000472748.5:n.490+57T=
ENST00000475360.6:c.313+57T=	ENSP00000437845.1:n.313+57T=
NM_003705.4:c.325+57T=	NP_003696.2:n.325+57T=
NR_047549.1:n.302-11269T=
XM_005246923.3:c.274+57T=	XP_005246980.1:n.274+57T=
XM_011512069.1:c.325+57T=	XP_011510371.1:n.325+57T=
XM_011512070.1:c.-53+57T=	XP_011510372.1:n.-53+57T=
XM_011512070.3:c.-53+57T=	XP_011510372.1:n.-53+57T=
NM_003705.5:c.325+57T= MANE Select	NP_003696.2:n.325+57T=
NR_047549.2:n.240-11269T=