Canonical Allele Identifier: CA916710162

Gene: SLC25A12

Linked Data

• dbSNP Id: rs1558933212

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171856136del , CM000664.2:g.171856136del	GRCh38
NC_000002.11:g.172712646del , CM000664.1:g.172712646del	GRCh37
NC_000002.10:g.172420892del	NCBI36
NG_011781.1:g.43171del
NG_011781.2:g.43171del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.210-184del MANE Select	ENSP00000388658.2:n.210-184del
ENST00000263812.8:c.210-11625del	ENSP00000263812.4:n.210-11625del
ENST00000422440.6:c.210-184del	ENSP00000388658.2:n.210-184del
ENST00000426896.5:c.210-184del	ENSP00000413968.1:n.210-184del
ENST00000464063.1:n.531-184del
ENST00000472748.5:n.375-184del
ENST00000475360.6:c.198-184del	ENSP00000437845.1:n.198-184del
ENST00000484227.5:n.408-184del
NM_003705.4:c.210-184del	NP_003696.2:n.210-184del
NR_047549.1:n.302-11625del
XM_005246923.3:c.159-184del	XP_005246980.1:n.159-184del
XM_011512069.1:c.210-184del	XP_011510371.1:n.210-184del
XM_011512070.1:c.-168-184del	XP_011510372.1:n.-168-184del
XM_011512070.3:c.-168-184del	XP_011510372.1:n.-168-184del
NM_003705.5:c.210-184del MANE Select	NP_003696.2:n.210-184del
NR_047549.2:n.240-11625del