Canonical Allele Identifier: CA197543962

Gene: TMEM245

Linked Data

• dbSNP Id: rs943017235
• gnomAD v3: 9-109053092-T-A
• gnomAD v4: 9-109053092-T-A
• MyVariant Identifiers: chr9:g.111815372T>A (hg19) ; chr9:g.109053092T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.109053092T>A , CM000671.2:g.109053092T>A	GRCh38
NC_000009.11:g.111815372T>A , CM000671.1:g.111815372T>A	GRCh37
NC_000009.10:g.110855193T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000413712.7:c.1831-2400A>T	ENSP00000394798.3:n.1831-2400A>T
ENST00000374586.8:c.1855-2400A>T MANE Select	ENSP00000363714.3:n.1855-2400A>T
ENST00000374586.7:c.1855-2400A>T	ENSP00000363714.3:n.1855-2400A>T
ENST00000413712.6:c.632-2400A>T
ENST00000491854.1:c.*427-2400A>T	ENSP00000417842.1:n.*427-2400A>T
NM_032012.3:c.1855-2400A>T	NP_114401.2:n.1855-2400A>T
XM_011518446.1:c.1852-2400A>T	XP_011516748.1:n.1852-2400A>T
XM_011518447.1:c.1831-2400A>T	XP_011516749.1:n.1831-2400A>T
XM_011518448.1:c.1750-2400A>T	XP_011516750.1:n.1750-2400A>T
XM_011518449.1:c.1738-2400A>T	XP_011516751.1:n.1738-2400A>T
XM_011518450.1:c.1735-2400A>T	XP_011516752.1:n.1735-2400A>T
XM_011518451.1:c.1726-2400A>T	XP_011516753.1:n.1726-2400A>T
XM_011518452.1:c.1621-2400A>T	XP_011516754.1:n.1621-2400A>T
XR_930240.1:n.1392-21201T>A
XM_011518446.2:c.1852-2400A>T	XP_011516748.1:n.1852-2400A>T
XM_011518449.2:c.1738-2400A>T	XP_011516751.1:n.1738-2400A>T
XM_011518452.2:c.1621-2400A>T	XP_011516754.1:n.1621-2400A>T
XM_017014571.1:c.1828-2400A>T	XP_016870060.1:n.1828-2400A>T
XM_017014572.1:c.1597-2400A>T	XP_016870061.1:n.1597-2400A>T
NM_032012.4:c.1855-2400A>T MANE Select	NP_114401.2:n.1855-2400A>T