Canonical Allele Identifier: CA858450465

Gene: TMEM245

Linked Data

• dbSNP Id: rs1242090299
• gnomAD v3: 9-109053200-CG-C
• gnomAD v4: 9-109053200-CG-C
• MyVariant Identifiers: chr9:g.111815481del (hg19) ; chr9:g.109053201del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.109053202del , CM000671.2:g.109053202del	GRCh38
NC_000009.11:g.111815482del , CM000671.1:g.111815482del	GRCh37
NC_000009.10:g.110855303del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413712.7:c.1831-2509del	ENSP00000394798.3:n.1831-2509del
ENST00000374586.8:c.1855-2509del MANE Select	ENSP00000363714.3:n.1855-2509del
ENST00000374586.7:c.1855-2509del	ENSP00000363714.3:n.1855-2509del
ENST00000413712.6:c.632-2509del
ENST00000491854.1:c.*427-2509del	ENSP00000417842.1:n.*427-2509del
NM_032012.3:c.1855-2509del	NP_114401.2:n.1855-2509del
XM_011518446.1:c.1852-2509del	XP_011516748.1:n.1852-2509del
XM_011518447.1:c.1831-2509del	XP_011516749.1:n.1831-2509del
XM_011518448.1:c.1750-2509del	XP_011516750.1:n.1750-2509del
XM_011518449.1:c.1738-2509del	XP_011516751.1:n.1738-2509del
XM_011518450.1:c.1735-2509del	XP_011516752.1:n.1735-2509del
XM_011518451.1:c.1726-2509del	XP_011516753.1:n.1726-2509del
XM_011518452.1:c.1621-2509del	XP_011516754.1:n.1621-2509del
XR_930240.1:n.1392-21091del
XM_011518446.2:c.1852-2509del	XP_011516748.1:n.1852-2509del
XM_011518449.2:c.1738-2509del	XP_011516751.1:n.1738-2509del
XM_011518452.2:c.1621-2509del	XP_011516754.1:n.1621-2509del
XM_017014571.1:c.1828-2509del	XP_016870060.1:n.1828-2509del
XM_017014572.1:c.1597-2509del	XP_016870061.1:n.1597-2509del
NM_032012.4:c.1855-2509del MANE Select	NP_114401.2:n.1855-2509del