Canonical Allele Identifier: CA1316747719

Gene: TMEFF2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.192049679_192049698delinsCAAGATTTCAAAAGCAAGCA , CM000664.2:g.192049679_192049698delinsCAAGATTTCAAAAGCAAGCA	GRCh38
NC_000002.11:g.192914405_192914424delinsCAAGATTTCAAAAGCAAGCA , CM000664.1:g.192914405_192914424delinsCAAGATTTCAAAAGCAAGCA	GRCh37
NC_000002.10:g.192622650_192622669delinsCAAGATTTCAAAAGCAAGCA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000272771.10:c.536+7981_536+8000delinsTGCTTGCTTTTGAAATCTTG MANE Select	ENSP00000272771.5:n.536+7981_536+8000deli...
ENST00000272771.9:c.536+7981_536+8000delinsTGCTTGCTTTTGAAATCTTG	ENSP00000272771.5:n.536+7981_536+8000deli...
ENST00000392314.5:c.536+7981_536+8000delinsTGCTTGCTTTTGAAATCTTG	ENSP00000376128.1:n.536+7981_536+8000deli...
NM_001305134.1:c.536+7981_536+8000delinsTGCTTGCTTTTGAAATCTTG	NP_001292063.1:n.536+7981_536+8000delinsT...
NM_016192.2:c.536+7981_536+8000delinsTGCTTGCTTTTGAAATCTTG	NP_057276.2:n.536+7981_536+8000delinsTGCT...
NM_016192.3:c.536+7981_536+8000delinsTGCTTGCTTTTGAAATCTTG	NP_057276.2:n.536+7981_536+8000delinsTGCT...
XM_005246437.2:c.536+7981_536+8000delinsTGCTTGCTTTTGAAATCTTG	XP_005246494.1:n.536+7981_536+8000delinsT...
XM_011510890.1:c.509+7981_509+8000delinsTGCTTGCTTTTGAAATCTTG	XP_011509192.1:n.509+7981_509+8000delinsT...
XR_923721.1:n.171+831_171+850delinsCAAGATTTCAAAAGCAAGCA
XR_923722.1:n.171+831_171+850delinsCAAGATTTCAAAAGCAAGCA
XM_011510890.3:c.509+7981_509+8000delinsTGCTTGCTTTTGAAATCTTG	XP_011509192.1:n.509+7981_509+8000delinsT...
XM_017003739.2:c.509+7981_509+8000delinsTGCTTGCTTTTGAAATCTTG	XP_016859228.1:n.509+7981_509+8000delinsT...
XM_017003740.2:c.536+7981_536+8000delinsTGCTTGCTTTTGAAATCTTG	XP_016859229.1:n.536+7981_536+8000delinsT...
XR_001739830.1:n.171+831_171+850delinsCAAGATTTCAAAAGCAAGCA
NM_016192.4:c.536+7981_536+8000delinsTGCTTGCTTTTGAAATCTTG MANE Select	NP_057276.2:n.536+7981_536+8000delinsTGCT...
NM_001305134.2:c.536+7981_536+8000delinsTGCTTGCTTTTGAAATCTTG	NP_001292063.1:n.536+7981_536+8000delinsT...