Canonical Allele Identifier: CA10856908

Gene: TRAF5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.211329427A>G , CM000663.2:g.211329427A>G	GRCh38
NC_000001.10:g.211502769A>G , CM000663.1:g.211502769A>G	GRCh37
NC_000001.9:g.209569392A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261464.10:c.-2+2538A>G MANE Select	ENSP00000261464.5:n.-2+2538A>G
ENST00000261464.9:c.-2+2538A>G	ENSP00000261464.5:n.-2+2538A>G
ENST00000336184.6:c.-2+2754A>G	ENSP00000336825.2:n.-2+2754A>G
ENST00000462410.5:n.59+2754A>G
ENST00000488428.1:n.192+2538A>G
ENST00000494355.1:n.57+2538A>G
NM_001033910.2:c.-2+2538A>G	NP_001029082.1:n.-2+2538A>G
NM_004619.3:c.-2+2754A>G	NP_004610.1:n.-2+2754A>G
XM_011509956.1:c.191+2538A>G	XP_011508258.1:n.191+2538A>G
XM_011509957.1:c.191+2538A>G	XP_011508259.1:n.191+2538A>G
XM_011509958.1:c.191+2538A>G	XP_011508260.1:n.191+2538A>G
XM_011509960.1:c.-2+2754A>G	XP_011508262.1:n.-2+2754A>G
NM_001319207.1:c.-2+2538A>G	NP_001306136.1:n.-2+2538A>G
XM_011509957.3:c.191+2538A>G	XP_011508259.1:n.191+2538A>G
XM_011509960.3:c.-2+2754A>G	XP_011508262.1:n.-2+2754A>G
XM_024449459.1:c.191+2538A>G	XP_024305227.1:n.191+2538A>G
NM_001033910.3:c.-2+2538A>G MANE Select	NP_001029082.1:n.-2+2538A>G
NM_001319207.2:c.-2+2538A>G	NP_001306136.1:n.-2+2538A>G
NM_004619.4:c.-2+2754A>G	NP_004610.1:n.-2+2754A>G