Canonical Allele Identifier: CA844193591

Gene: SLC25A13

Linked Data

• dbSNP Id: rs749337707
• gnomAD v3: 7-96189546-T-A
• gnomAD v4: 7-96189546-T-A
• MyVariant Identifiers: chr7:g.95818858T>A (hg19) ; chr7:g.96189546T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189546T>A , CM000669.2:g.96189546T>A	GRCh38
NC_000007.13:g.95818858T>A , CM000669.1:g.95818858T>A	GRCh37
NC_000007.12:g.95656794T>A	NCBI36
NG_012247.1:g.137602A>T
NG_012247.2:g.137602A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.848+35A>T MANE Select	ENSP00000265631.6:n.848+35A>T
ENST00000265631.9:c.848+35A>T	ENSP00000265631.5:n.848+35A>T
ENST00000416240.6:c.848+35A>T	ENSP00000400101.2:n.848+35A>T
NM_001160210.1:c.848+35A>T	NP_001153682.1:n.848+35A>T
NM_014251.2:c.848+35A>T	NP_055066.1:n.848+35A>T
NR_027662.1:n.923+35A>T
XM_006715831.2:c.881+35A>T	XP_006715894.1:n.881+35A>T
XM_011515727.1:c.881+35A>T	XP_011514029.1:n.881+35A>T
XM_011515728.1:c.-4-168A>T	XP_011514030.1:n.-4-168A>T
XM_006715831.4:c.881+35A>T	XP_006715894.1:n.881+35A>T
XM_011515727.3:c.881+35A>T	XP_011514029.1:n.881+35A>T
XM_017011663.1:c.839+35A>T	XP_016867152.1:n.839+35A>T
XM_017011664.2:c.-4-168A>T	XP_016867153.1:n.-4-168A>T
XM_017011665.1:c.-4-168A>T	XP_016867154.1:n.-4-168A>T
XR_001744525.2:n.1019+35A>T
XR_002956405.1:n.1161+35A>T
NM_014251.3:c.848+35A>T MANE Select	NP_055066.1:n.848+35A>T
NR_027662.2:n.874+35A>T
NM_001160210.2:c.848+35A>T	NP_001153682.1:n.848+35A>T