Canonical Allele Identifier: CA1307543824

Gene: SLC25A12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171856092_171856096delinsTAAGG , CM000664.2:g.171856092_171856096delinsTAAGG	GRCh38
NC_000002.11:g.172712602_172712606delinsTAAGG , CM000664.1:g.172712602_172712606delinsTAAGG	GRCh37
NC_000002.10:g.172420848_172420852delinsTAAGG	NCBI36
NG_011781.1:g.43208_43212delinsCCTTA
NG_011781.2:g.43208_43212delinsCCTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.210-147_210-143delinsCCTTA MANE Select	ENSP00000388658.2:n.210-147_210-143delinsCCTTA
ENST00000263812.8:c.210-11588_210-11584delinsCCTTA	ENSP00000263812.4:n.210-11588_210-11584delinsCCTTA
ENST00000422440.6:c.210-147_210-143delinsCCTTA	ENSP00000388658.2:n.210-147_210-143delinsCCTTA
ENST00000426896.5:c.210-147_210-143delinsCCTTA	ENSP00000413968.1:n.210-147_210-143delinsCCTTA
ENST00000464063.1:n.531-147_531-143delinsCCTTA
ENST00000472748.5:n.375-147_375-143delinsCCTTA
ENST00000475360.6:c.198-147_198-143delinsCCTTA	ENSP00000437845.1:n.198-147_198-143delinsCCTTA
ENST00000484227.5:n.408-147_408-143delinsCCTTA
NM_003705.4:c.210-147_210-143delinsCCTTA	NP_003696.2:n.210-147_210-143delinsCCTTA
NR_047549.1:n.302-11588_302-11584delinsCCTTA
XM_005246923.3:c.159-147_159-143delinsCCTTA	XP_005246980.1:n.159-147_159-143delinsCCTTA
XM_011512069.1:c.210-147_210-143delinsCCTTA	XP_011510371.1:n.210-147_210-143delinsCCTTA
XM_011512070.1:c.-168-147_-168-143delinsCCTTA	XP_011510372.1:n.-168-147_-168-143delinsCCTTA
XM_011512070.3:c.-168-147_-168-143delinsCCTTA	XP_011510372.1:n.-168-147_-168-143delinsCCTTA
NM_003705.5:c.210-147_210-143delinsCCTTA MANE Select	NP_003696.2:n.210-147_210-143delinsCCTTA
NR_047549.2:n.240-11588_240-11584delinsCCTTA