Canonical Allele Identifier: CA1871405461

Gene: TMEM245

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.109053231_109053232delinsGC , CM000671.2:g.109053231_109053232delinsGC	GRCh38
NC_000009.11:g.111815511_111815512delinsGC , CM000671.1:g.111815511_111815512delinsGC	GRCh37
NC_000009.10:g.110855332_110855333delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413712.7:c.1831-2540_1831-2539delinsGC	ENSP00000394798.3:n.1831-2540_1831-2539delinsGC
ENST00000374586.8:c.1855-2540_1855-2539delinsGC MANE Select	ENSP00000363714.3:n.1855-2540_1855-2539delinsGC
ENST00000374586.7:c.1855-2540_1855-2539delinsGC	ENSP00000363714.3:n.1855-2540_1855-2539delinsGC
ENST00000413712.6:c.632-2540_632-2539delinsGC
ENST00000491854.1:c.*427-2540_*427-2539delinsGC	ENSP00000417842.1:n.*427-2540_*427-2539delinsGC
NM_032012.3:c.1855-2540_1855-2539delinsGC	NP_114401.2:n.1855-2540_1855-2539delinsGC
XM_011518446.1:c.1852-2540_1852-2539delinsGC	XP_011516748.1:n.1852-2540_1852-2539delinsGC
XM_011518447.1:c.1831-2540_1831-2539delinsGC	XP_011516749.1:n.1831-2540_1831-2539delinsGC
XM_011518448.1:c.1750-2540_1750-2539delinsGC	XP_011516750.1:n.1750-2540_1750-2539delinsGC
XM_011518449.1:c.1738-2540_1738-2539delinsGC	XP_011516751.1:n.1738-2540_1738-2539delinsGC
XM_011518450.1:c.1735-2540_1735-2539delinsGC	XP_011516752.1:n.1735-2540_1735-2539delinsGC
XM_011518451.1:c.1726-2540_1726-2539delinsGC	XP_011516753.1:n.1726-2540_1726-2539delinsGC
XM_011518452.1:c.1621-2540_1621-2539delinsGC	XP_011516754.1:n.1621-2540_1621-2539delinsGC
XR_930240.1:n.1392-21062_1392-21061delinsGC
XM_011518446.2:c.1852-2540_1852-2539delinsGC	XP_011516748.1:n.1852-2540_1852-2539delinsGC
XM_011518449.2:c.1738-2540_1738-2539delinsGC	XP_011516751.1:n.1738-2540_1738-2539delinsGC
XM_011518452.2:c.1621-2540_1621-2539delinsGC	XP_011516754.1:n.1621-2540_1621-2539delinsGC
XM_017014571.1:c.1828-2540_1828-2539delinsGC	XP_016870060.1:n.1828-2540_1828-2539delinsGC
XM_017014572.1:c.1597-2540_1597-2539delinsGC	XP_016870061.1:n.1597-2540_1597-2539delinsGC
NM_032012.4:c.1855-2540_1855-2539delinsGC MANE Select	NP_114401.2:n.1855-2540_1855-2539delinsGC