Canonical Allele Identifier: CA1871405329

Gene: TMEM245

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.109052918_109052919delinsCA , CM000671.2:g.109052918_109052919delinsCA	GRCh38
NC_000009.11:g.111815198_111815199delinsCA , CM000671.1:g.111815198_111815199delinsCA	GRCh37
NC_000009.10:g.110855019_110855020delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413712.7:c.1831-2227_1831-2226delinsTG	ENSP00000394798.3:n.1831-2227_1831-2226delinsTG
ENST00000374586.8:c.1855-2227_1855-2226delinsTG MANE Select	ENSP00000363714.3:n.1855-2227_1855-2226delinsTG
ENST00000374586.7:c.1855-2227_1855-2226delinsTG	ENSP00000363714.3:n.1855-2227_1855-2226delinsTG
ENST00000413712.6:c.632-2227_632-2226delinsTG
ENST00000491854.1:c.*427-2227_*427-2226delinsTG	ENSP00000417842.1:n.*427-2227_*427-2226delinsTG
NM_032012.3:c.1855-2227_1855-2226delinsTG	NP_114401.2:n.1855-2227_1855-2226delinsTG
XM_011518446.1:c.1852-2227_1852-2226delinsTG	XP_011516748.1:n.1852-2227_1852-2226delinsTG
XM_011518447.1:c.1831-2227_1831-2226delinsTG	XP_011516749.1:n.1831-2227_1831-2226delinsTG
XM_011518448.1:c.1750-2227_1750-2226delinsTG	XP_011516750.1:n.1750-2227_1750-2226delinsTG
XM_011518449.1:c.1738-2227_1738-2226delinsTG	XP_011516751.1:n.1738-2227_1738-2226delinsTG
XM_011518450.1:c.1735-2227_1735-2226delinsTG	XP_011516752.1:n.1735-2227_1735-2226delinsTG
XM_011518451.1:c.1726-2227_1726-2226delinsTG	XP_011516753.1:n.1726-2227_1726-2226delinsTG
XM_011518452.1:c.1621-2227_1621-2226delinsTG	XP_011516754.1:n.1621-2227_1621-2226delinsTG
XR_930240.1:n.1392-21375_1392-21374delinsCA
XM_011518446.2:c.1852-2227_1852-2226delinsTG	XP_011516748.1:n.1852-2227_1852-2226delinsTG
XM_011518449.2:c.1738-2227_1738-2226delinsTG	XP_011516751.1:n.1738-2227_1738-2226delinsTG
XM_011518452.2:c.1621-2227_1621-2226delinsTG	XP_011516754.1:n.1621-2227_1621-2226delinsTG
XM_017014571.1:c.1828-2227_1828-2226delinsTG	XP_016870060.1:n.1828-2227_1828-2226delinsTG
XM_017014572.1:c.1597-2227_1597-2226delinsTG	XP_016870061.1:n.1597-2227_1597-2226delinsTG
NM_032012.4:c.1855-2227_1855-2226delinsTG MANE Select	NP_114401.2:n.1855-2227_1855-2226delinsTG