Canonical Allele Identifier: CA858450384

Gene: TMEM245

Linked Data

• dbSNP Id: rs1323951682
• gnomAD v3: 9-109053033-TTA-T
• gnomAD v4: 9-109053033-TTA-T
• MyVariant Identifiers: chr9:g.111815314_111815315del (hg19) ; chr9:g.109053034_109053035del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.109053037_109053038del , CM000671.2:g.109053037_109053038del	GRCh38
NC_000009.11:g.111815317_111815318del , CM000671.1:g.111815317_111815318del	GRCh37
NC_000009.10:g.110855138_110855139del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000413712.7:c.1831-2343_1831-2342del	ENSP00000394798.3:n.1831-2343_1831-2342del
ENST00000374586.8:c.1855-2343_1855-2342del MANE Select	ENSP00000363714.3:n.1855-2343_1855-2342del
ENST00000374586.7:c.1855-2343_1855-2342del	ENSP00000363714.3:n.1855-2343_1855-2342del
ENST00000413712.6:c.632-2343_632-2342del
ENST00000491854.1:c.*427-2343_*427-2342del	ENSP00000417842.1:n.*427-2343_*427-2342del
NM_032012.3:c.1855-2343_1855-2342del	NP_114401.2:n.1855-2343_1855-2342del
XM_011518446.1:c.1852-2343_1852-2342del	XP_011516748.1:n.1852-2343_1852-2342del
XM_011518447.1:c.1831-2343_1831-2342del	XP_011516749.1:n.1831-2343_1831-2342del
XM_011518448.1:c.1750-2343_1750-2342del	XP_011516750.1:n.1750-2343_1750-2342del
XM_011518449.1:c.1738-2343_1738-2342del	XP_011516751.1:n.1738-2343_1738-2342del
XM_011518450.1:c.1735-2343_1735-2342del	XP_011516752.1:n.1735-2343_1735-2342del
XM_011518451.1:c.1726-2343_1726-2342del	XP_011516753.1:n.1726-2343_1726-2342del
XM_011518452.1:c.1621-2343_1621-2342del	XP_011516754.1:n.1621-2343_1621-2342del
XR_930240.1:n.1392-21256_1392-21255del
XM_011518446.2:c.1852-2343_1852-2342del	XP_011516748.1:n.1852-2343_1852-2342del
XM_011518449.2:c.1738-2343_1738-2342del	XP_011516751.1:n.1738-2343_1738-2342del
XM_011518452.2:c.1621-2343_1621-2342del	XP_011516754.1:n.1621-2343_1621-2342del
XM_017014571.1:c.1828-2343_1828-2342del	XP_016870060.1:n.1828-2343_1828-2342del
XM_017014572.1:c.1597-2343_1597-2342del	XP_016870061.1:n.1597-2343_1597-2342del
NM_032012.4:c.1855-2343_1855-2342del MANE Select	NP_114401.2:n.1855-2343_1855-2342del