Canonical Allele Identifier: CA2740867878

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189545_96189546insAAAAA , CM000669.2:g.96189545_96189546insAAAAA	GRCh38
NC_000007.13:g.95818857_95818858insAAAAA , CM000669.1:g.95818857_95818858insAAAAA	GRCh37
NC_000007.12:g.95656793_95656794insAAAAA	NCBI36
NG_012247.1:g.137602_137603insTTTTT
NG_012247.2:g.137602_137603insTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.848+35_848+36insTTTTT MANE Select	ENSP00000265631.6:n.848+35_848+36insTTTTT
ENST00000265631.9:c.848+35_848+36insTTTTT	ENSP00000265631.5:n.848+35_848+36insTTTTT
ENST00000416240.6:c.848+35_848+36insTTTTT	ENSP00000400101.2:n.848+35_848+36insTTTTT
NM_001160210.1:c.848+35_848+36insTTTTT	NP_001153682.1:n.848+35_848+36insTTTTT
NM_014251.2:c.848+35_848+36insTTTTT	NP_055066.1:n.848+35_848+36insTTTTT
NR_027662.1:n.923+35_923+36insTTTTT
XM_006715831.2:c.881+35_881+36insTTTTT	XP_006715894.1:n.881+35_881+36insTTTTT
XM_011515727.1:c.881+35_881+36insTTTTT	XP_011514029.1:n.881+35_881+36insTTTTT
XM_011515728.1:c.-4-168_-4-167insTTTTT	XP_011514030.1:n.-4-168_-4-167insTTTTT
XM_006715831.4:c.881+35_881+36insTTTTT	XP_006715894.1:n.881+35_881+36insTTTTT
XM_011515727.3:c.881+35_881+36insTTTTT	XP_011514029.1:n.881+35_881+36insTTTTT
XM_017011663.1:c.839+35_839+36insTTTTT	XP_016867152.1:n.839+35_839+36insTTTTT
XM_017011664.2:c.-4-168_-4-167insTTTTT	XP_016867153.1:n.-4-168_-4-167insTTTTT
XM_017011665.1:c.-4-168_-4-167insTTTTT	XP_016867154.1:n.-4-168_-4-167insTTTTT
XR_001744525.2:n.1019+35_1019+36insTTTTT
XR_002956405.1:n.1161+35_1161+36insTTTTT
NM_014251.3:c.848+35_848+36insTTTTT MANE Select	NP_055066.1:n.848+35_848+36insTTTTT
NR_027662.2:n.874+35_874+36insTTTTT
NM_001160210.2:c.848+35_848+36insTTTTT	NP_001153682.1:n.848+35_848+36insTTTTT