Canonical Allele Identifier: CA1307543828

Gene: SLC25A12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171856096_171856101delinsGAAGGA , CM000664.2:g.171856096_171856101delinsGAAGGA	GRCh38
NC_000002.11:g.172712606_172712611delinsGAAGGA , CM000664.1:g.172712606_172712611delinsGAAGGA	GRCh37
NC_000002.10:g.172420852_172420857delinsGAAGGA	NCBI36
NG_011781.1:g.43203_43208delinsTCCTTC
NG_011781.2:g.43203_43208delinsTCCTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.210-152_210-147delinsTCCTTC MANE Select	ENSP00000388658.2:n.210-152_210-147delinsTCCTTC
ENST00000263812.8:c.210-11593_210-11588delinsTCCTTC	ENSP00000263812.4:n.210-11593_210-11588delinsTCCTTC
ENST00000422440.6:c.210-152_210-147delinsTCCTTC	ENSP00000388658.2:n.210-152_210-147delinsTCCTTC
ENST00000426896.5:c.210-152_210-147delinsTCCTTC	ENSP00000413968.1:n.210-152_210-147delinsTCCTTC
ENST00000464063.1:n.531-152_531-147delinsTCCTTC
ENST00000472748.5:n.375-152_375-147delinsTCCTTC
ENST00000475360.6:c.198-152_198-147delinsTCCTTC	ENSP00000437845.1:n.198-152_198-147delinsTCCTTC
ENST00000484227.5:n.408-152_408-147delinsTCCTTC
NM_003705.4:c.210-152_210-147delinsTCCTTC	NP_003696.2:n.210-152_210-147delinsTCCTTC
NR_047549.1:n.302-11593_302-11588delinsTCCTTC
XM_005246923.3:c.159-152_159-147delinsTCCTTC	XP_005246980.1:n.159-152_159-147delinsTCCTTC
XM_011512069.1:c.210-152_210-147delinsTCCTTC	XP_011510371.1:n.210-152_210-147delinsTCCTTC
XM_011512070.1:c.-168-152_-168-147delinsTCCTTC	XP_011510372.1:n.-168-152_-168-147delinsTCCTTC
XM_011512070.3:c.-168-152_-168-147delinsTCCTTC	XP_011510372.1:n.-168-152_-168-147delinsTCCTTC
NM_003705.5:c.210-152_210-147delinsTCCTTC MANE Select	NP_003696.2:n.210-152_210-147delinsTCCTTC
NR_047549.2:n.240-11593_240-11588delinsTCCTTC