Canonical Allele Identifier: CA2661928385

Gene: SLC25A12

Linked Data

• gnomAD v4: 2-171855654-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171855654T>A , CM000664.2:g.171855654T>A	GRCh38
NC_000002.11:g.172712164T>A , CM000664.1:g.172712164T>A	GRCh37
NC_000002.10:g.172420410T>A	NCBI36
NG_011781.1:g.43650A>T
NG_011781.2:g.43650A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.325+180A>T MANE Select	ENSP00000388658.2:n.325+180A>T
ENST00000263812.8:c.210-11146A>T	ENSP00000263812.4:n.210-11146A>T
ENST00000422440.6:c.325+180A>T	ENSP00000388658.2:n.325+180A>T
ENST00000426896.5:c.325+180A>T	ENSP00000413968.1:n.325+180A>T
ENST00000472748.5:n.490+180A>T
ENST00000475360.6:c.313+180A>T	ENSP00000437845.1:n.313+180A>T
NM_003705.4:c.325+180A>T	NP_003696.2:n.325+180A>T
NR_047549.1:n.302-11146A>T
XM_005246923.3:c.274+180A>T	XP_005246980.1:n.274+180A>T
XM_011512069.1:c.325+180A>T	XP_011510371.1:n.325+180A>T
XM_011512070.1:c.-53+180A>T	XP_011510372.1:n.-53+180A>T
XM_011512070.3:c.-53+180A>T	XP_011510372.1:n.-53+180A>T
NM_003705.5:c.325+180A>T MANE Select	NP_003696.2:n.325+180A>T
NR_047549.2:n.240-11146A>T