Canonical Allele Identifier: CA349632395

Gene: SLC25A12

Linked Data

• dbSNP Id: rs1229549255
• gnomAD v2: 2-172712403-G-T
• gnomAD v4: 2-171855893-G-T
• MyVariant Identifiers: chr2:g.172712403G>T (hg19) ; chr2:g.171855893G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171855893G>T , CM000664.2:g.171855893G>T	GRCh38
NC_000002.11:g.172712403G>T , CM000664.1:g.172712403G>T	GRCh37
NC_000002.10:g.172420649G>T	NCBI36
NG_011781.1:g.43411C>A
NG_011781.2:g.43411C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.266C>A MANE Select	ENSP00000388658.2:p.Ser89Tyr
ENST00000263812.8:c.210-11385C>A	ENSP00000263812.4:n.210-11385C>A
ENST00000422440.6:c.266C>A	ENSP00000388658.2:p.Ser89Tyr
ENST00000426896.5:c.266C>A	ENSP00000413968.1:p.Ser89Tyr
ENST00000472748.5:n.431C>A
ENST00000475360.6:c.254C>A	ENSP00000437845.1:p.Ser85Tyr
ENST00000484227.5:n.464C>A
NM_003705.4:c.266C>A	NP_003696.2:p.Ser89Tyr
NR_047549.1:n.302-11385C>A
XM_005246923.3:c.215C>A	XP_005246980.1:p.Ser72Tyr
XM_011512069.1:c.266C>A	XP_011510371.1:p.Ser89Tyr
XM_011512070.1:c.-112C>A	XP_011510372.1:n.-112C>A
XM_011512070.3:c.-112C>A	XP_011510372.1:n.-112C>A
NM_003705.5:c.266C>A MANE Select	NP_003696.2:p.Ser89Tyr
NR_047549.2:n.240-11385C>A