Canonical Allele Identifier: CA2661928498

Gene: SLC25A12

Linked Data

• gnomAD v4: 2-171856035-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171856035C>T , CM000664.2:g.171856035C>T	GRCh38
NC_000002.11:g.172712545C>T , CM000664.1:g.172712545C>T	GRCh37
NC_000002.10:g.172420791C>T	NCBI36
NG_011781.1:g.43269G>A
NG_011781.2:g.43269G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.210-86G>A MANE Select	ENSP00000388658.2:n.210-86G>A
ENST00000263812.8:c.210-11527G>A	ENSP00000263812.4:n.210-11527G>A
ENST00000422440.6:c.210-86G>A	ENSP00000388658.2:n.210-86G>A
ENST00000426896.5:c.210-86G>A	ENSP00000413968.1:n.210-86G>A
ENST00000464063.1:n.531-86G>A
ENST00000472748.5:n.375-86G>A
ENST00000475360.6:c.198-86G>A	ENSP00000437845.1:n.198-86G>A
ENST00000484227.5:n.408-86G>A
NM_003705.4:c.210-86G>A	NP_003696.2:n.210-86G>A
NR_047549.1:n.302-11527G>A
XM_005246923.3:c.159-86G>A	XP_005246980.1:n.159-86G>A
XM_011512069.1:c.210-86G>A	XP_011510371.1:n.210-86G>A
XM_011512070.1:c.-168-86G>A	XP_011510372.1:n.-168-86G>A
XM_011512070.3:c.-168-86G>A	XP_011510372.1:n.-168-86G>A
NM_003705.5:c.210-86G>A MANE Select	NP_003696.2:n.210-86G>A
NR_047549.2:n.240-11527G>A