Canonical Allele Identifier: CA13770732

Gene: MTERF2 TMEM263

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.106973447T>C , CM000674.2:g.106973447T>C	GRCh38
NC_000012.11:g.107367225T>C , CM000674.1:g.107367225T>C	GRCh37
NC_000012.10:g.105891355T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713581.1:c.*4110A>G (MTERF2)	ENSP00000518873.1:n.*4110A>G
ENST00000280756.9:c.*2056T>C (TMEM263) MANE Select	ENSP00000280756.4:n.*2056T>C
ENST00000280756.8:c.*2056T>C (TMEM263)	ENSP00000280756.4:n.*2056T>C
ENST00000548125.5:c.*2056T>C (TMEM263)	ENSP00000449785.1:n.*2056T>C
ENST00000548806.1:n.215+1804T>C (TMEM263)
ENST00000551237.1:n.174-1504T>C (TMEM263)
NM_152261.2:c.*2056T>C (TMEM263)	NP_689474.1:n.*2056T>C
XM_011538965.1:c.*2056T>C (TMEM263)	XP_011537267.1:n.*2056T>C
NM_001319661.1:c.*2056T>C (TMEM263)	NP_001306590.1:n.*2056T>C
NM_001319662.1:c.*2056T>C (TMEM263)	NP_001306591.1:n.*2056T>C
NM_001319663.1:c.*2056T>C (TMEM263)	NP_001306592.1:n.*2056T>C
NM_001319664.1:c.*2056T>C (TMEM263)	NP_001306593.1:n.*2056T>C
NM_001319666.1:c.*2056T>C (TMEM263)	NP_001306595.1:n.*2056T>C
NM_152261.3:c.*2056T>C (TMEM263)	NP_689474.1:n.*2056T>C
XM_017019985.2:c.*4110A>G (MTERF2)	XP_016875474.1:n.*4110A>G
NM_152261.4:c.*2056T>C (TMEM263) MANE Select	NP_689474.1:n.*2056T>C
NM_001319661.2:c.*2056T>C (TMEM263)	NP_001306590.1:n.*2056T>C
NM_001319662.2:c.*2056T>C (TMEM263)	NP_001306591.1:n.*2056T>C
NM_001319663.2:c.*2056T>C (TMEM263)	NP_001306592.1:n.*2056T>C
NM_001319664.2:c.*2056T>C (TMEM263)	NP_001306593.1:n.*2056T>C
NM_001319666.2:c.*2056T>C (TMEM263)	NP_001306595.1:n.*2056T>C