Canonical Allele Identifier: CA1307543843

Gene: SLC25A12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171856131_171856132delinsAG , CM000664.2:g.171856131_171856132delinsAG	GRCh38
NC_000002.11:g.172712641_172712642delinsAG , CM000664.1:g.172712641_172712642delinsAG	GRCh37
NC_000002.10:g.172420887_172420888delinsAG	NCBI36
NG_011781.1:g.43172_43173delinsCT
NG_011781.2:g.43172_43173delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.210-183_210-182delinsCT MANE Select	ENSP00000388658.2:n.210-183_210-182delinsCT
ENST00000263812.8:c.210-11624_210-11623delinsCT	ENSP00000263812.4:n.210-11624_210-11623delinsCT
ENST00000422440.6:c.210-183_210-182delinsCT	ENSP00000388658.2:n.210-183_210-182delinsCT
ENST00000426896.5:c.210-183_210-182delinsCT	ENSP00000413968.1:n.210-183_210-182delinsCT
ENST00000464063.1:n.531-183_531-182delinsCT
ENST00000472748.5:n.375-183_375-182delinsCT
ENST00000475360.6:c.198-183_198-182delinsCT	ENSP00000437845.1:n.198-183_198-182delinsCT
ENST00000484227.5:n.408-183_408-182delinsCT
NM_003705.4:c.210-183_210-182delinsCT	NP_003696.2:n.210-183_210-182delinsCT
NR_047549.1:n.302-11624_302-11623delinsCT
XM_005246923.3:c.159-183_159-182delinsCT	XP_005246980.1:n.159-183_159-182delinsCT
XM_011512069.1:c.210-183_210-182delinsCT	XP_011510371.1:n.210-183_210-182delinsCT
XM_011512070.1:c.-168-183_-168-182delinsCT	XP_011510372.1:n.-168-183_-168-182delinsCT
XM_011512070.3:c.-168-183_-168-182delinsCT	XP_011510372.1:n.-168-183_-168-182delinsCT
NM_003705.5:c.210-183_210-182delinsCT MANE Select	NP_003696.2:n.210-183_210-182delinsCT
NR_047549.2:n.240-11624_240-11623delinsCT