Canonical Allele Identifier: CA1307526656

Gene: SLC25A12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171816943G= , CM000664.2:g.171816943G=	GRCh38
NC_000002.11:g.172673453G= , CM000664.1:g.172673453G=	GRCh37
NC_000002.10:g.172381699G=	NCBI36
NG_011781.1:g.82361C=
NG_011781.2:g.82361C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.931-1741C= MANE Select	ENSP00000388658.2:n.931-1741C=
ENST00000263812.8:c.*551-1741C=	ENSP00000263812.4:n.*551-1741C=
ENST00000422440.6:c.931-1741C=	ENSP00000388658.2:n.931-1741C=
ENST00000485880.1:n.459-1741C=
NM_003705.4:c.931-1741C=	NP_003696.2:n.931-1741C=
NR_047549.1:n.907-1741C=
XM_005246923.3:c.880-1741C=	XP_005246980.1:n.880-1741C=
XM_011512069.1:c.931-1741C=	XP_011510371.1:n.931-1741C=
XM_011512070.1:c.658-1741C=	XP_011510372.1:n.658-1741C=
XM_011512070.3:c.658-1741C=	XP_011510372.1:n.658-1741C=
NM_003705.5:c.931-1741C= MANE Select	NP_003696.2:n.931-1741C=
NR_047549.2:n.845-1741C=