Canonical Allele Identifier: CA1871405396
Gene: TMEM245 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.109053106_109053108delinsCAA , CM000671.2:g.109053106_109053108delinsCAA GRCh38
NC_000009.11:g.111815386_111815388delinsCAA , CM000671.1:g.111815386_111815388delinsCAA GRCh37
NC_000009.10:g.110855207_110855209delinsCAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000413712.7:c.1831-2416_1831-2414delinsTTG ENSP00000394798.3:n.1831-2416_1831-2414de...
ENST00000374586.8:c.1855-2416_1855-2414delinsTTG MANE Select ENSP00000363714.3:n.1855-2416_1855-2414de...
ENST00000374586.7:c.1855-2416_1855-2414delinsTTG ENSP00000363714.3:n.1855-2416_1855-2414de...
ENST00000413712.6:c.632-2416_632-2414delinsTTG
ENST00000491854.1:c.*427-2416_*427-2414delinsTTG ENSP00000417842.1:n.*427-2416_*427-2414de...
NM_032012.3:c.1855-2416_1855-2414delinsTTG NP_114401.2:n.1855-2416_1855-2414delinsTT...
XM_011518446.1:c.1852-2416_1852-2414delinsTTG XP_011516748.1:n.1852-2416_1852-2414delin...
XM_011518447.1:c.1831-2416_1831-2414delinsTTG XP_011516749.1:n.1831-2416_1831-2414delin...
XM_011518448.1:c.1750-2416_1750-2414delinsTTG XP_011516750.1:n.1750-2416_1750-2414delin...
XM_011518449.1:c.1738-2416_1738-2414delinsTTG XP_011516751.1:n.1738-2416_1738-2414delin...
XM_011518450.1:c.1735-2416_1735-2414delinsTTG XP_011516752.1:n.1735-2416_1735-2414delin...
XM_011518451.1:c.1726-2416_1726-2414delinsTTG XP_011516753.1:n.1726-2416_1726-2414delin...
XM_011518452.1:c.1621-2416_1621-2414delinsTTG XP_011516754.1:n.1621-2416_1621-2414delin...
XR_930240.1:n.1392-21187_1392-21185delinsCAA
XM_011518446.2:c.1852-2416_1852-2414delinsTTG XP_011516748.1:n.1852-2416_1852-2414delin...
XM_011518449.2:c.1738-2416_1738-2414delinsTTG XP_011516751.1:n.1738-2416_1738-2414delin...
XM_011518452.2:c.1621-2416_1621-2414delinsTTG XP_011516754.1:n.1621-2416_1621-2414delin...
XM_017014571.1:c.1828-2416_1828-2414delinsTTG XP_016870060.1:n.1828-2416_1828-2414delin...
XM_017014572.1:c.1597-2416_1597-2414delinsTTG XP_016870061.1:n.1597-2416_1597-2414delin...
NM_032012.4:c.1855-2416_1855-2414delinsTTG MANE Select NP_114401.2:n.1855-2416_1855-2414delinsTT...