Canonical Allele Identifier: CA1316747831

Gene: TMEFF2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.192049896G= , CM000664.2:g.192049896G=	GRCh38
NC_000002.11:g.192914622G= , CM000664.1:g.192914622G=	GRCh37
NC_000002.10:g.192622867G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272771.10:c.536+7783C= MANE Select	ENSP00000272771.5:n.536+7783C=
ENST00000272771.9:c.536+7783C=	ENSP00000272771.5:n.536+7783C=
ENST00000392314.5:c.536+7783C=	ENSP00000376128.1:n.536+7783C=
NM_001305134.1:c.536+7783C=	NP_001292063.1:n.536+7783C=
NM_016192.2:c.536+7783C=	NP_057276.2:n.536+7783C=
NM_016192.3:c.536+7783C=	NP_057276.2:n.536+7783C=
XM_005246437.2:c.536+7783C=	XP_005246494.1:n.536+7783C=
XM_011510890.1:c.509+7783C=	XP_011509192.1:n.509+7783C=
XR_923721.1:n.172-708G=
XR_923722.1:n.172-708G=
XM_011510890.3:c.509+7783C=	XP_011509192.1:n.509+7783C=
XM_017003739.2:c.509+7783C=	XP_016859228.1:n.509+7783C=
XM_017003740.2:c.536+7783C=	XP_016859229.1:n.536+7783C=
XR_001739830.1:n.172-708G=
NM_016192.4:c.536+7783C= MANE Select	NP_057276.2:n.536+7783C=
NM_001305134.2:c.536+7783C=	NP_001292063.1:n.536+7783C=