Canonical Allele Identifier: CA414660855

Gene: SLC25A14

Linked Data

• MyVariant Identifiers: chrX:g.129480664G>A (hg19) ; chrX:g.130346690G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.130346690G>A , CM000685.2:g.130346690G>A	GRCh38
NC_000023.10:g.129480664G>A , CM000685.1:g.129480664G>A	GRCh37
NC_000023.9:g.129308345G>A	NCBI36
NG_012850.1:g.11618G>A
NG_012850.2:g.11618G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545805.6:c.316G>A MANE Select	ENSP00000444642.2:p.Gly106Arg
ENST00000218197.9:c.316G>A	ENSP00000218197.5:p.Gly106Arg
ENST00000339231.3:c.307G>A	ENSP00000342797.3:p.Gly103Arg
ENST00000361980.9:c.307G>A	ENSP00000354455.5:p.Gly103Arg
ENST00000424447.5:c.316G>A	ENSP00000402578.1:p.Gly106Arg
ENST00000464184.5:n.307G>A
ENST00000464342.5:n.308G>A
ENST00000467346.1:n.237G>A
ENST00000467496.5:n.461G>A
ENST00000478474.5:n.91+1415G>A
ENST00000495156.5:n.318G>A
ENST00000543953.5:c.211G>A	ENSP00000445225.2:p.Gly71Arg
ENST00000545805.5:c.316G>A	ENSP00000444642.2:p.Gly106Arg
ENST00000612248.4:c.307G>A	ENSP00000477981.1:p.Gly103Arg
NM_001282195.1:c.316G>A	NP_001269124.1:p.Gly106Arg
NM_001282196.1:c.307G>A	NP_001269125.1:p.Gly103Arg
NM_001282197.1:c.307G>A	NP_001269126.1:p.Gly103Arg
NM_001282198.1:c.211G>A	NP_001269127.1:p.Gly71Arg
NR_104107.1:n.330G>A
XM_005262489.3:c.15-2561G>A	XP_005262546.1:n.15-2561G>A
XM_011531402.1:c.343G>A	XP_011529704.1:p.Gly115Arg
XM_011531403.1:c.211G>A	XP_011529705.1:p.Gly71Arg
XM_011531404.1:c.307G>A	XP_011529706.1:p.Gly103Arg
XM_011531405.1:c.211G>A	XP_011529707.1:p.Gly71Arg
XM_005262489.5:c.15-2561G>A	XP_005262546.1:n.15-2561G>A
XM_011531402.2:c.343G>A	XP_011529704.1:p.Gly115Arg
XM_017029936.2:c.211G>A	XP_016885425.1:p.Gly71Arg
XM_017029937.1:c.343G>A	XP_016885426.1:p.Gly115Arg
XM_017029938.2:c.316G>A	XP_016885427.1:p.Gly106Arg
XM_017029939.2:c.307G>A	XP_016885428.1:p.Gly103Arg
XM_017029940.1:c.15-2561G>A	XP_016885429.1:n.15-2561G>A
XM_017029941.1:c.-161G>A	XP_016885430.1:n.-161G>A
XM_017029942.1:c.-116+1415G>A	XP_016885431.1:n.-116+1415G>A
XM_017029943.1:c.-101-2561G>A	XP_016885432.1:n.-101-2561G>A
XM_024452474.1:c.316G>A	XP_024308242.1:p.Gly106Arg
NM_001282195.2:c.316G>A MANE Select	NP_001269124.1:p.Gly106Arg
NM_001282196.2:c.307G>A	NP_001269125.1:p.Gly103Arg
NR_104107.2:n.299G>A
NM_001282197.2:c.307G>A	NP_001269126.1:p.Gly103Arg
NM_001282198.2:c.211G>A	NP_001269127.1:p.Gly71Arg