Canonical Allele Identifier: CA1307543745

Gene: SLC25A12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171855907T= , CM000664.2:g.171855907T=	GRCh38
NC_000002.11:g.172712417T= , CM000664.1:g.172712417T=	GRCh37
NC_000002.10:g.172420663T=	NCBI36
NG_011781.1:g.43397A=
NG_011781.2:g.43397A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000422440.7:c.252A= MANE Select	ENSP00000388658.2:p.Leu84=
ENST00000263812.8:c.210-11399A=	ENSP00000263812.4:n.210-11399A=
ENST00000422440.6:c.252A=	ENSP00000388658.2:p.Leu84=
ENST00000426896.5:c.252A=	ENSP00000413968.1:p.Leu84=
ENST00000472748.5:n.417A=
ENST00000475360.6:c.240A=	ENSP00000437845.1:p.Leu80=
ENST00000484227.5:n.450A=
NM_003705.4:c.252A=	NP_003696.2:p.Leu84=
NR_047549.1:n.302-11399A=
XM_005246923.3:c.201A=	XP_005246980.1:p.Leu67=
XM_011512069.1:c.252A=	XP_011510371.1:p.Leu84=
XM_011512070.1:c.-126A=	XP_011510372.1:n.-126A=
XM_011512070.3:c.-126A=	XP_011510372.1:n.-126A=
NM_003705.5:c.252A= MANE Select	NP_003696.2:p.Leu84=
NR_047549.2:n.240-11399A=