Canonical Allele Identifier: CA1307534450

Gene: SLC25A12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171833670T= , CM000664.2:g.171833670T=	GRCh38
NC_000002.11:g.172690180T= , CM000664.1:g.172690180T=	GRCh37
NC_000002.10:g.172398426T=	NCBI36
NG_011781.1:g.65634A=
NG_011781.2:g.65634A=

Transcript Alleles

HGVS	Amino-acid Change
NM_003705.5:c.845+293A= MANE Select	NP_003696.2:n.845+293A=
ENST00000422440.7:c.845+293A= MANE Select	ENSP00000388658.2:n.845+293A=
NM_003705.4:c.845+293A=	NP_003696.2:n.845+293A=
NR_047549.1:n.821+293A=
NR_047549.2:n.759+293A=
ENST00000263812.8:c.*465+293A=	ENSP00000263812.4:n.*465+293A=
ENST00000422440.6:c.845+293A=	ENSP00000388658.2:n.845+293A=
ENST00000485880.1:n.373+293A=
XM_005246923.3:c.794+293A=	XP_005246980.1:n.794+293A=
XM_011512069.1:c.845+293A=	XP_011510371.1:n.845+293A=
XM_011512070.1:c.572+293A=	XP_011510372.1:n.572+293A=
XM_011512070.3:c.572+293A=	XP_011510372.1:n.572+293A=