Canonical Allele Identifier: CA1307543636
Gene: SLC25A12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.171855596_171855598delinsGTA , CM000664.2:g.171855596_171855598delinsGTA GRCh38
NC_000002.11:g.172712106_172712108delinsGTA , CM000664.1:g.172712106_172712108delinsGTA GRCh37
NC_000002.10:g.172420352_172420354delinsGTA NCBI36
NG_011781.1:g.43706_43708delinsTAC
NG_011781.2:g.43706_43708delinsTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000422440.7:c.325+236_325+238delinsTAC MANE Select ENSP00000388658.2:n.325+236_325+238delinsTAC
ENST00000263812.8:c.210-11090_210-11088delinsTAC ENSP00000263812.4:n.210-11090_210-11088delinsTAC
ENST00000422440.6:c.325+236_325+238delinsTAC ENSP00000388658.2:n.325+236_325+238delinsTAC
ENST00000426896.5:c.325+236_325+238delinsTAC ENSP00000413968.1:n.325+236_325+238delinsTAC
ENST00000472748.5:n.490+236_490+238delinsTAC
ENST00000475360.6:c.313+236_313+238delinsTAC ENSP00000437845.1:n.313+236_313+238delinsTAC
NM_003705.4:c.325+236_325+238delinsTAC NP_003696.2:n.325+236_325+238delinsTAC
NR_047549.1:n.302-11090_302-11088delinsTAC
XM_005246923.3:c.274+236_274+238delinsTAC XP_005246980.1:n.274+236_274+238delinsTAC
XM_011512069.1:c.325+236_325+238delinsTAC XP_011510371.1:n.325+236_325+238delinsTAC
XM_011512070.1:c.-53+236_-53+238delinsTAC XP_011510372.1:n.-53+236_-53+238delinsTAC
XM_011512070.3:c.-53+236_-53+238delinsTAC XP_011510372.1:n.-53+236_-53+238delinsTAC
NM_003705.5:c.325+236_325+238delinsTAC MANE Select NP_003696.2:n.325+236_325+238delinsTAC
NR_047549.2:n.240-11090_240-11088delinsTAC