Canonical Allele Identifier: CA1871405409

Gene: TMEM245

Linked Data

• dbSNP Id: rs1828734504

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.109053128_109053129insTT , CM000671.2:g.109053128_109053129insTT	GRCh38
NC_000009.11:g.111815408_111815409insTT , CM000671.1:g.111815408_111815409insTT	GRCh37
NC_000009.10:g.110855229_110855230insTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413712.7:c.1831-2437_1831-2436insAA	ENSP00000394798.3:n.1831-2437_1831-2436insAA
ENST00000374586.8:c.1855-2437_1855-2436insAA MANE Select	ENSP00000363714.3:n.1855-2437_1855-2436insAA
ENST00000374586.7:c.1855-2437_1855-2436insAA	ENSP00000363714.3:n.1855-2437_1855-2436insAA
ENST00000413712.6:c.632-2437_632-2436insAA
ENST00000491854.1:c.*427-2437_*427-2436insAA	ENSP00000417842.1:n.*427-2437_*427-2436insAA
NM_032012.3:c.1855-2437_1855-2436insAA	NP_114401.2:n.1855-2437_1855-2436insAA
XM_011518446.1:c.1852-2437_1852-2436insAA	XP_011516748.1:n.1852-2437_1852-2436insAA
XM_011518447.1:c.1831-2437_1831-2436insAA	XP_011516749.1:n.1831-2437_1831-2436insAA
XM_011518448.1:c.1750-2437_1750-2436insAA	XP_011516750.1:n.1750-2437_1750-2436insAA
XM_011518449.1:c.1738-2437_1738-2436insAA	XP_011516751.1:n.1738-2437_1738-2436insAA
XM_011518450.1:c.1735-2437_1735-2436insAA	XP_011516752.1:n.1735-2437_1735-2436insAA
XM_011518451.1:c.1726-2437_1726-2436insAA	XP_011516753.1:n.1726-2437_1726-2436insAA
XM_011518452.1:c.1621-2437_1621-2436insAA	XP_011516754.1:n.1621-2437_1621-2436insAA
XR_930240.1:n.1392-21165_1392-21164insTT
XM_011518446.2:c.1852-2437_1852-2436insAA	XP_011516748.1:n.1852-2437_1852-2436insAA
XM_011518449.2:c.1738-2437_1738-2436insAA	XP_011516751.1:n.1738-2437_1738-2436insAA
XM_011518452.2:c.1621-2437_1621-2436insAA	XP_011516754.1:n.1621-2437_1621-2436insAA
XM_017014571.1:c.1828-2437_1828-2436insAA	XP_016870060.1:n.1828-2437_1828-2436insAA
XM_017014572.1:c.1597-2437_1597-2436insAA	XP_016870061.1:n.1597-2437_1597-2436insAA
NM_032012.4:c.1855-2437_1855-2436insAA MANE Select	NP_114401.2:n.1855-2437_1855-2436insAA