Canonical Allele Identifier: CA2694690285

Gene: SLC25A14

Linked Data

• gnomAD v4: X-130346748-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.130346752del , CM000685.2:g.130346752del	GRCh38
NC_000023.10:g.129480726del , CM000685.1:g.129480726del	GRCh37
NC_000023.9:g.129308407del	NCBI36
NG_012850.1:g.11680del
NG_012850.2:g.11680del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545805.6:c.317+61del MANE Select	ENSP00000444642.2:n.317+61del
ENST00000218197.9:c.317+61del	ENSP00000218197.5:n.317+61del
ENST00000339231.3:c.308+61del	ENSP00000342797.3:n.308+61del
ENST00000361980.9:c.308+61del	ENSP00000354455.5:n.308+61del
ENST00000424447.5:c.317+61del	ENSP00000402578.1:n.317+61del
ENST00000464184.5:n.308+61del
ENST00000464342.5:n.309+61del
ENST00000467346.1:n.238+61del
ENST00000467496.5:n.462+61del
ENST00000478474.5:n.91+1477del
ENST00000495156.5:n.319+61del
ENST00000543953.5:c.212+61del	ENSP00000445225.2:n.212+61del
ENST00000545805.5:c.317+61del	ENSP00000444642.2:n.317+61del
ENST00000612248.4:c.308+61del	ENSP00000477981.1:n.308+61del
NM_001282195.1:c.317+61del	NP_001269124.1:n.317+61del
NM_001282196.1:c.308+61del	NP_001269125.1:n.308+61del
NM_001282197.1:c.308+61del	NP_001269126.1:n.308+61del
NM_001282198.1:c.212+61del	NP_001269127.1:n.212+61del
NR_104107.1:n.331+61del
XM_005262489.3:c.15-2499del	XP_005262546.1:n.15-2499del
XM_011531402.1:c.344+61del	XP_011529704.1:n.344+61del
XM_011531403.1:c.212+61del	XP_011529705.1:n.212+61del
XM_011531404.1:c.308+61del	XP_011529706.1:n.308+61del
XM_011531405.1:c.212+61del	XP_011529707.1:n.212+61del
XM_005262489.5:c.15-2499del	XP_005262546.1:n.15-2499del
XM_011531402.2:c.344+61del	XP_011529704.1:n.344+61del
XM_017029936.2:c.212+61del	XP_016885425.1:n.212+61del
XM_017029937.1:c.344+61del	XP_016885426.1:n.344+61del
XM_017029938.2:c.317+61del	XP_016885427.1:n.317+61del
XM_017029939.2:c.308+61del	XP_016885428.1:n.308+61del
XM_017029940.1:c.15-2499del	XP_016885429.1:n.15-2499del
XM_017029941.1:c.-160+61del	XP_016885430.1:n.-160+61del
XM_017029942.1:c.-116+1477del	XP_016885431.1:n.-116+1477del
XM_017029943.1:c.-101-2499del	XP_016885432.1:n.-101-2499del
XM_024452474.1:c.317+61del	XP_024308242.1:n.317+61del
NM_001282195.2:c.317+61del MANE Select	NP_001269124.1:n.317+61del
NM_001282196.2:c.308+61del	NP_001269125.1:n.308+61del
NR_104107.2:n.300+61del
NM_001282197.2:c.308+61del	NP_001269126.1:n.308+61del
NM_001282198.2:c.212+61del	NP_001269127.1:n.212+61del