Canonical Allele Identifier: CA844156328

Gene: SLC25A13

Linked Data

• dbSNP Id: rs80338726
• MyVariant Identifiers: chr7:g.95751008_95751009insTTT (hg19) ; chr7:g.96121696_96121697insTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121697_96121698insTTT , CM000669.2:g.96121697_96121698insTTT	GRCh38
NC_000007.13:g.95751009_95751010insTTT , CM000669.1:g.95751009_95751010insTTT	GRCh37
NC_000007.12:g.95588945_95588946insTTT	NCBI36
NG_012247.1:g.205451_205452insAAA
NG_012247.2:g.205451_205452insAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1799_1800insAAA MANE Select	ENSP00000265631.6:p.Tyr600Ter
ENST00000265631.9:c.1799_1800insAAA	ENSP00000265631.5:p.Tyr600Ter
ENST00000416240.6:c.1802_1803insAAA	ENSP00000400101.2:p.Tyr601Ter
ENST00000494085.1:n.302_303insAAA
NM_001160210.1:c.1802_1803insAAA	NP_001153682.1:p.Tyr601Ter
NM_014251.2:c.1799_1800insAAA	NP_055066.1:p.Tyr600Ter
NR_027662.1:n.1874_1875insAAA
XM_006715831.2:c.1832_1833insAAA	XP_006715894.1:p.Tyr611Ter
XM_011515728.1:c.947_948insAAA	XP_011514030.1:p.Tyr316Ter
XM_006715831.4:c.1832_1833insAAA	XP_006715894.1:p.Tyr611Ter
XM_017011663.1:c.1790_1791insAAA	XP_016867152.1:p.Tyr597Ter
XM_017011664.2:c.947_948insAAA	XP_016867153.1:p.Tyr316Ter
XM_017011665.1:c.947_948insAAA	XP_016867154.1:p.Tyr316Ter
XR_001744525.2:n.2045_2046insAAA
XR_002956405.1:n.2603_2604insAAA
NM_014251.3:c.1799_1800insAAA MANE Select	NP_055066.1:p.Tyr600Ter
NR_027662.2:n.1825_1826insAAA
NM_001160210.2:c.1802_1803insAAA	NP_001153682.1:p.Tyr601Ter