Canonical Allele Identifier: CA2577157810

Gene: SLC25A12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171855808_171855814del , CM000664.2:g.171855808_171855814del	GRCh38
NC_000002.11:g.172712318_172712324del , CM000664.1:g.172712318_172712324del	GRCh37
NC_000002.10:g.172420564_172420570del	NCBI36
NG_011781.1:g.43496_43502del
NG_011781.2:g.43496_43502del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.325+26_325+32del MANE Select	ENSP00000388658.2:n.325+26_325+32del
ENST00000263812.8:c.210-11300_210-11294del	ENSP00000263812.4:n.210-11300_210-11294del
ENST00000422440.6:c.325+26_325+32del	ENSP00000388658.2:n.325+26_325+32del
ENST00000426896.5:c.325+26_325+32del	ENSP00000413968.1:n.325+26_325+32del
ENST00000472748.5:n.490+26_490+32del
ENST00000475360.6:c.313+26_313+32del	ENSP00000437845.1:n.313+26_313+32del
ENST00000484227.5:n.549_555del
NM_003705.4:c.325+26_325+32del	NP_003696.2:n.325+26_325+32del
NR_047549.1:n.302-11300_302-11294del
XM_005246923.3:c.274+26_274+32del	XP_005246980.1:n.274+26_274+32del
XM_011512069.1:c.325+26_325+32del	XP_011510371.1:n.325+26_325+32del
XM_011512070.1:c.-53+26_-53+32del	XP_011510372.1:n.-53+26_-53+32del
XM_011512070.3:c.-53+26_-53+32del	XP_011510372.1:n.-53+26_-53+32del
NM_003705.5:c.325+26_325+32del MANE Select	NP_003696.2:n.325+26_325+32del
NR_047549.2:n.240-11300_240-11294del