Canonical Allele Identifier: CA2753172178

Gene: SLC25A12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171856105_171856107del , CM000664.2:g.171856105_171856107del	GRCh38
NC_000002.11:g.172712615_172712617del , CM000664.1:g.172712615_172712617del	GRCh37
NC_000002.10:g.172420861_172420863del	NCBI36
NG_011781.1:g.43199_43201del
NG_011781.2:g.43199_43201del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.210-156_210-154del MANE Select	ENSP00000388658.2:n.210-156_210-154del
ENST00000263812.8:c.210-11597_210-11595del	ENSP00000263812.4:n.210-11597_210-11595del
ENST00000422440.6:c.210-156_210-154del	ENSP00000388658.2:n.210-156_210-154del
ENST00000426896.5:c.210-156_210-154del	ENSP00000413968.1:n.210-156_210-154del
ENST00000464063.1:n.531-156_531-154del
ENST00000472748.5:n.375-156_375-154del
ENST00000475360.6:c.198-156_198-154del	ENSP00000437845.1:n.198-156_198-154del
ENST00000484227.5:n.408-156_408-154del
NM_003705.4:c.210-156_210-154del	NP_003696.2:n.210-156_210-154del
NR_047549.1:n.302-11597_302-11595del
XM_005246923.3:c.159-156_159-154del	XP_005246980.1:n.159-156_159-154del
XM_011512069.1:c.210-156_210-154del	XP_011510371.1:n.210-156_210-154del
XM_011512070.1:c.-168-156_-168-154del	XP_011510372.1:n.-168-156_-168-154del
XM_011512070.3:c.-168-156_-168-154del	XP_011510372.1:n.-168-156_-168-154del
NM_003705.5:c.210-156_210-154del MANE Select	NP_003696.2:n.210-156_210-154del
NR_047549.2:n.240-11597_240-11595del