Canonical Allele Identifier: CA368258239

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95751225T>C (hg19) ; chr7:g.96121913T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121913T>C , CM000669.2:g.96121913T>C	GRCh38
NC_000007.13:g.95751225T>C , CM000669.1:g.95751225T>C	GRCh37
NC_000007.12:g.95589161T>C	NCBI36
NG_012247.1:g.205235A>G
NG_012247.2:g.205235A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1676A>G MANE Select	ENSP00000265631.6:p.Tyr559Cys
ENST00000265631.9:c.1676A>G	ENSP00000265631.5:p.Tyr559Cys
ENST00000416240.6:c.1679A>G	ENSP00000400101.2:p.Tyr560Cys
ENST00000494085.1:n.86A>G
NM_001160210.1:c.1679A>G	NP_001153682.1:p.Tyr560Cys
NM_014251.2:c.1676A>G	NP_055066.1:p.Tyr559Cys
NR_027662.1:n.1751A>G
XM_006715831.2:c.1709A>G	XP_006715894.1:p.Tyr570Cys
XM_011515728.1:c.824A>G	XP_011514030.1:p.Tyr275Cys
XM_006715831.4:c.1709A>G	XP_006715894.1:p.Tyr570Cys
XM_017011663.1:c.1667A>G	XP_016867152.1:p.Tyr556Cys
XM_017011664.2:c.824A>G	XP_016867153.1:p.Tyr275Cys
XM_017011665.1:c.824A>G	XP_016867154.1:p.Tyr275Cys
XR_001744525.2:n.1922A>G
XR_002956405.1:n.2480A>G
NM_014251.3:c.1676A>G MANE Select	NP_055066.1:p.Tyr559Cys
NR_027662.2:n.1702A>G
NM_001160210.2:c.1679A>G	NP_001153682.1:p.Tyr560Cys