Canonical Allele Identifier: CA1307543713

Gene: SLC25A12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171855816_171855819delinsATCT , CM000664.2:g.171855816_171855819delinsATCT	GRCh38
NC_000002.11:g.172712326_172712329delinsATCT , CM000664.1:g.172712326_172712329delinsATCT	GRCh37
NC_000002.10:g.172420572_172420575delinsATCT	NCBI36
NG_011781.1:g.43485_43488delinsAGAT
NG_011781.2:g.43485_43488delinsAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.325+15_325+18delinsAGAT MANE Select	ENSP00000388658.2:n.325+15_325+18delinsAGAT
ENST00000263812.8:c.210-11311_210-11308delinsAGAT	ENSP00000263812.4:n.210-11311_210-11308delinsAGAT
ENST00000422440.6:c.325+15_325+18delinsAGAT	ENSP00000388658.2:n.325+15_325+18delinsAGAT
ENST00000426896.5:c.325+15_325+18delinsAGAT	ENSP00000413968.1:n.325+15_325+18delinsAGAT
ENST00000472748.5:n.490+15_490+18delinsAGAT
ENST00000475360.6:c.313+15_313+18delinsAGAT	ENSP00000437845.1:n.313+15_313+18delinsAGAT
ENST00000484227.5:n.538_541delinsAGAT
NM_003705.4:c.325+15_325+18delinsAGAT	NP_003696.2:n.325+15_325+18delinsAGAT
NR_047549.1:n.302-11311_302-11308delinsAGAT
XM_005246923.3:c.274+15_274+18delinsAGAT	XP_005246980.1:n.274+15_274+18delinsAGAT
XM_011512069.1:c.325+15_325+18delinsAGAT	XP_011510371.1:n.325+15_325+18delinsAGAT
XM_011512070.1:c.-53+15_-53+18delinsAGAT	XP_011510372.1:n.-53+15_-53+18delinsAGAT
XM_011512070.3:c.-53+15_-53+18delinsAGAT	XP_011510372.1:n.-53+15_-53+18delinsAGAT
NM_003705.5:c.325+15_325+18delinsAGAT MANE Select	NP_003696.2:n.325+15_325+18delinsAGAT
NR_047549.2:n.240-11311_240-11308delinsAGAT