Canonical Allele Identifier: CA368260082

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95813606A>G (hg19) ; chr7:g.96184294A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96184294A>G , CM000669.2:g.96184294A>G	GRCh38
NC_000007.13:g.95813606A>G , CM000669.1:g.95813606A>G	GRCh37
NC_000007.12:g.95651542A>G	NCBI36
NG_012247.1:g.142854T>C
NG_012247.2:g.142854T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1160T>C MANE Select	ENSP00000265631.6:p.Phe387Ser
ENST00000265631.9:c.1160T>C	ENSP00000265631.5:p.Phe387Ser
ENST00000416240.6:c.1163T>C	ENSP00000400101.2:p.Phe388Ser
ENST00000484495.5:n.313T>C
ENST00000490072.5:n.227T>C
ENST00000492869.1:n.281T>C
NM_001160210.1:c.1163T>C	NP_001153682.1:p.Phe388Ser
NM_014251.2:c.1160T>C	NP_055066.1:p.Phe387Ser
NR_027662.1:n.1235T>C
XM_006715831.2:c.1193T>C	XP_006715894.1:p.Phe398Ser
XM_011515727.1:c.1193T>C	XP_011514029.1:p.Phe398Ser
XM_011515728.1:c.308T>C	XP_011514030.1:p.Phe103Ser
XM_006715831.4:c.1193T>C	XP_006715894.1:p.Phe398Ser
XM_011515727.3:c.1193T>C	XP_011514029.1:p.Phe398Ser
XM_017011663.1:c.1151T>C	XP_016867152.1:p.Phe384Ser
XM_017011664.2:c.308T>C	XP_016867153.1:p.Phe103Ser
XM_017011665.1:c.308T>C	XP_016867154.1:p.Phe103Ser
XR_001744525.2:n.1331T>C
XR_002956405.1:n.1964T>C
NM_014251.3:c.1160T>C MANE Select	NP_055066.1:p.Phe387Ser
NR_027662.2:n.1186T>C
NM_001160210.2:c.1163T>C	NP_001153682.1:p.Phe388Ser