Canonical Allele Identifier: CA1871423565

Gene: TMEM245

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.109091966G= , CM000671.2:g.109091966G=	GRCh38
NC_000009.11:g.111854246G= , CM000671.1:g.111854246G=	GRCh37
NC_000009.10:g.110894067G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_032012.4:c.917-811C= MANE Select	NP_114401.2:n.917-811C=
ENST00000374586.8:c.917-811C= MANE Select	ENSP00000363714.3:n.917-811C=
NM_032012.3:c.917-811C=	NP_114401.2:n.917-811C=
ENST00000374586.7:c.917-811C=	ENSP00000363714.3:n.917-811C=
ENST00000413712.7:c.917-811C=	ENSP00000394798.3:n.917-811C=
ENST00000491854.1:c.167-811C=	ENSP00000417842.1:n.167-811C=
XM_011518446.1:c.917-814C=	XP_011516748.1:n.917-814C=
XM_011518446.2:c.917-814C=	XP_011516748.1:n.917-814C=
XM_011518447.1:c.917-811C=	XP_011516749.1:n.917-811C=
XM_011518448.1:c.917-811C=	XP_011516750.1:n.917-811C=
XM_011518449.1:c.800-811C=	XP_011516751.1:n.800-811C=
XM_011518449.2:c.800-811C=	XP_011516751.1:n.800-811C=
XM_011518450.1:c.800-814C=	XP_011516752.1:n.800-814C=
XM_011518451.1:c.917-811C=	XP_011516753.1:n.917-811C=
XM_011518452.1:c.916+1509C=	XP_011516754.1:n.916+1509C=
XM_011518452.2:c.916+1509C=	XP_011516754.1:n.916+1509C=
XM_017014571.1:c.917-814C=	XP_016870060.1:n.917-814C=
XM_017014572.1:c.916+1509C=	XP_016870061.1:n.916+1509C=