Canonical Allele Identifier: CA349632438

Gene: SLC25A12

Linked Data

• MyVariant Identifiers: chr2:g.172712407C>T (hg19) ; chr2:g.171855897C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171855897C>T , CM000664.2:g.171855897C>T	GRCh38
NC_000002.11:g.172712407C>T , CM000664.1:g.172712407C>T	GRCh37
NC_000002.10:g.172420653C>T	NCBI36
NG_011781.1:g.43407G>A
NG_011781.2:g.43407G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000422440.7:c.262G>A MANE Select	ENSP00000388658.2:p.Asp88Asn
ENST00000263812.8:c.210-11389G>A	ENSP00000263812.4:n.210-11389G>A
ENST00000422440.6:c.262G>A	ENSP00000388658.2:p.Asp88Asn
ENST00000426896.5:c.262G>A	ENSP00000413968.1:p.Asp88Asn
ENST00000472748.5:n.427G>A
ENST00000475360.6:c.250G>A	ENSP00000437845.1:p.Asp84Asn
ENST00000484227.5:n.460G>A
NM_003705.4:c.262G>A	NP_003696.2:p.Asp88Asn
NR_047549.1:n.302-11389G>A
XM_005246923.3:c.211G>A	XP_005246980.1:p.Asp71Asn
XM_011512069.1:c.262G>A	XP_011510371.1:p.Asp88Asn
XM_011512070.1:c.-116G>A	XP_011510372.1:n.-116G>A
XM_011512070.3:c.-116G>A	XP_011510372.1:n.-116G>A
NM_003705.5:c.262G>A MANE Select	NP_003696.2:p.Asp88Asn
NR_047549.2:n.240-11389G>A