Canonical Allele Identifier: CA368263384

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95822405T>G (hg19) ; chr7:g.96193093T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96193093T>G , CM000669.2:g.96193093T>G	GRCh38
NC_000007.13:g.95822405T>G , CM000669.1:g.95822405T>G	GRCh37
NC_000007.12:g.95660341T>G	NCBI36
NG_012247.1:g.134055A>C
NG_012247.2:g.134055A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.559A>C MANE Select	ENSP00000265631.6:p.Met187Leu
ENST00000265631.9:c.559A>C	ENSP00000265631.5:p.Met187Leu
ENST00000416240.6:c.559A>C	ENSP00000400101.2:p.Met187Leu
NM_001160210.1:c.559A>C	NP_001153682.1:p.Met187Leu
NM_014251.2:c.559A>C	NP_055066.1:p.Met187Leu
NR_027662.1:n.634A>C
XM_006715831.2:c.592A>C	XP_006715894.1:p.Met198Leu
XM_011515727.1:c.592A>C	XP_011514029.1:p.Met198Leu
XM_006715831.4:c.592A>C	XP_006715894.1:p.Met198Leu
XM_011515727.3:c.592A>C	XP_011514029.1:p.Met198Leu
XM_017011663.1:c.550A>C	XP_016867152.1:p.Met184Leu
XM_017011664.2:c.-200A>C	XP_016867153.1:n.-200A>C
XM_017011665.1:c.-200A>C	XP_016867154.1:n.-200A>C
XR_001744525.2:n.730A>C
XR_002956405.1:n.872A>C
NM_014251.3:c.559A>C MANE Select	NP_055066.1:p.Met187Leu
NR_027662.2:n.585A>C
NM_001160210.2:c.559A>C	NP_001153682.1:p.Met187Leu