Canonical Allele Identifier: CA916710158

Gene: SLC25A12

Linked Data

• dbSNP Id: rs869228523

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171855597_171855598del , CM000664.2:g.171855597_171855598del	GRCh38
NC_000002.11:g.172712107_172712108del , CM000664.1:g.172712107_172712108del	GRCh37
NC_000002.10:g.172420353_172420354del	NCBI36
NG_011781.1:g.43706_43707del
NG_011781.2:g.43706_43707del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.325+236_325+237del MANE Select	ENSP00000388658.2:n.325+236_325+237del
ENST00000263812.8:c.210-11090_210-11089del	ENSP00000263812.4:n.210-11090_210-11089del
ENST00000422440.6:c.325+236_325+237del	ENSP00000388658.2:n.325+236_325+237del
ENST00000426896.5:c.325+236_325+237del	ENSP00000413968.1:n.325+236_325+237del
ENST00000472748.5:n.490+236_490+237del
ENST00000475360.6:c.313+236_313+237del	ENSP00000437845.1:n.313+236_313+237del
NM_003705.4:c.325+236_325+237del	NP_003696.2:n.325+236_325+237del
NR_047549.1:n.302-11090_302-11089del
XM_005246923.3:c.274+236_274+237del	XP_005246980.1:n.274+236_274+237del
XM_011512069.1:c.325+236_325+237del	XP_011510371.1:n.325+236_325+237del
XM_011512070.1:c.-53+236_-53+237del	XP_011510372.1:n.-53+236_-53+237del
XM_011512070.3:c.-53+236_-53+237del	XP_011510372.1:n.-53+236_-53+237del
NM_003705.5:c.325+236_325+237del MANE Select	NP_003696.2:n.325+236_325+237del
NR_047549.2:n.240-11090_240-11089del