Canonical Allele Identifier: CA2571913593

Gene: SLC25A12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171856007_171856008insG , CM000664.2:g.171856007_171856008insG	GRCh38
NC_000002.11:g.172712517_172712518insG , CM000664.1:g.172712517_172712518insG	GRCh37
NC_000002.10:g.172420763_172420764insG	NCBI36
NG_011781.1:g.43296_43297insC
NG_011781.2:g.43296_43297insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.210-59_210-58insC MANE Select	ENSP00000388658.2:n.210-59_210-58insC
ENST00000263812.8:c.210-11500_210-11499insC	ENSP00000263812.4:n.210-11500_210-11499insC
ENST00000422440.6:c.210-59_210-58insC	ENSP00000388658.2:n.210-59_210-58insC
ENST00000426896.5:c.210-59_210-58insC	ENSP00000413968.1:n.210-59_210-58insC
ENST00000464063.1:n.531-59_531-58insC
ENST00000472748.5:n.375-59_375-58insC
ENST00000475360.6:c.198-59_198-58insC	ENSP00000437845.1:n.198-59_198-58insC
ENST00000484227.5:n.408-59_408-58insC
NM_003705.4:c.210-59_210-58insC	NP_003696.2:n.210-59_210-58insC
NR_047549.1:n.302-11500_302-11499insC
XM_005246923.3:c.159-59_159-58insC	XP_005246980.1:n.159-59_159-58insC
XM_011512069.1:c.210-59_210-58insC	XP_011510371.1:n.210-59_210-58insC
XM_011512070.1:c.-168-59_-168-58insC	XP_011510372.1:n.-168-59_-168-58insC
XM_011512070.3:c.-168-59_-168-58insC	XP_011510372.1:n.-168-59_-168-58insC
NM_003705.5:c.210-59_210-58insC MANE Select	NP_003696.2:n.210-59_210-58insC
NR_047549.2:n.240-11500_240-11499insC