Canonical Allele Identifier: CA410636540

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19164168C>A (hg19) ; chr22:g.19176655C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176655C>A , CM000684.2:g.19176655C>A	GRCh38
NC_000022.10:g.19164168C>A , CM000684.1:g.19164168C>A	GRCh37
NC_000022.9:g.17544168C>A	NCBI36
NG_033863.1:g.7209G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.670G>T MANE Select	ENSP00000215882.5:p.Gly224Trp
ENST00000215882.9:c.670G>T	ENSP00000215882.5:p.Gly224Trp
ENST00000451283.5:c.361G>T	ENSP00000401480.1:p.Gly121Trp
ENST00000470922.5:n.812G>T
NM_001256534.1:c.691G>T	NP_001243463.1:p.Gly231Trp
NM_001287387.1:c.361G>T	NP_001274316.1:p.Gly121Trp
NM_005984.4:c.670G>T	NP_005975.1:p.Gly224Trp
NR_046298.2:n.721G>T
NM_005984.5:c.670G>T MANE Select	NP_005975.1:p.Gly224Trp
NM_001256534.2:c.691G>T	NP_001243463.1:p.Gly231Trp
NM_001287387.2:c.361G>T	NP_001274316.1:p.Gly121Trp
NR_046298.3:n.594G>T