Canonical Allele Identifier: CA1307543744

Gene: SLC25A12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171855905C= , CM000664.2:g.171855905C=	GRCh38
NC_000002.11:g.172712415C= , CM000664.1:g.172712415C=	GRCh37
NC_000002.10:g.172420661C=	NCBI36
NG_011781.1:g.43399G=
NG_011781.2:g.43399G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000422440.7:c.254G= MANE Select	ENSP00000388658.2:p.Cys85=
ENST00000263812.8:c.210-11397G=	ENSP00000263812.4:n.210-11397G=
ENST00000422440.6:c.254G=	ENSP00000388658.2:p.Cys85=
ENST00000426896.5:c.254G=	ENSP00000413968.1:p.Cys85=
ENST00000472748.5:n.419G=
ENST00000475360.6:c.242G=	ENSP00000437845.1:p.Cys81=
ENST00000484227.5:n.452G=
NM_003705.4:c.254G=	NP_003696.2:p.Cys85=
NR_047549.1:n.302-11397G=
XM_005246923.3:c.203G=	XP_005246980.1:p.Cys68=
XM_011512069.1:c.254G=	XP_011510371.1:p.Cys85=
XM_011512070.1:c.-124G=	XP_011510372.1:n.-124G=
XM_011512070.3:c.-124G=	XP_011510372.1:n.-124G=
NM_003705.5:c.254G= MANE Select	NP_003696.2:p.Cys85=
NR_047549.2:n.240-11397G=