Canonical Allele Identifier: CA1307543857

Gene: SLC25A12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171856148_171856149delinsTG , CM000664.2:g.171856148_171856149delinsTG	GRCh38
NC_000002.11:g.172712658_172712659delinsTG , CM000664.1:g.172712658_172712659delinsTG	GRCh37
NC_000002.10:g.172420904_172420905delinsTG	NCBI36
NG_011781.1:g.43155_43156delinsCA
NG_011781.2:g.43155_43156delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.210-200_210-199delinsCA MANE Select	ENSP00000388658.2:n.210-200_210-199delinsCA
ENST00000263812.8:c.210-11641_210-11640delinsCA	ENSP00000263812.4:n.210-11641_210-11640delinsCA
ENST00000422440.6:c.210-200_210-199delinsCA	ENSP00000388658.2:n.210-200_210-199delinsCA
ENST00000426896.5:c.210-200_210-199delinsCA	ENSP00000413968.1:n.210-200_210-199delinsCA
ENST00000464063.1:n.531-200_531-199delinsCA
ENST00000472748.5:n.375-200_375-199delinsCA
ENST00000475360.6:c.198-200_198-199delinsCA	ENSP00000437845.1:n.198-200_198-199delinsCA
ENST00000484227.5:n.408-200_408-199delinsCA
NM_003705.4:c.210-200_210-199delinsCA	NP_003696.2:n.210-200_210-199delinsCA
NR_047549.1:n.302-11641_302-11640delinsCA
XM_005246923.3:c.159-200_159-199delinsCA	XP_005246980.1:n.159-200_159-199delinsCA
XM_011512069.1:c.210-200_210-199delinsCA	XP_011510371.1:n.210-200_210-199delinsCA
XM_011512070.1:c.-168-200_-168-199delinsCA	XP_011510372.1:n.-168-200_-168-199delinsCA
XM_011512070.3:c.-168-200_-168-199delinsCA	XP_011510372.1:n.-168-200_-168-199delinsCA
NM_003705.5:c.210-200_210-199delinsCA MANE Select	NP_003696.2:n.210-200_210-199delinsCA
NR_047549.2:n.240-11641_240-11640delinsCA