Canonical Allele Identifier: CA2663893772

Gene: TRAF3IP1

Linked Data

• gnomAD v4: 2-238397681-TGGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397685_238397687del , CM000664.2:g.238397685_238397687del	GRCh38
NC_000002.11:g.239306326_239306328del , CM000664.1:g.239306326_239306328del	GRCh37
NC_000002.10:g.238971065_238971067del	NCBI36
NG_053055.1:g.82197_82199del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1910+6_1910+8del MANE Select	ENSP00000362424.4:n.1910+6_1910+8del
ENST00000373327.4:c.1910+6_1910+8del	ENSP00000362424.4:n.1910+6_1910+8del
ENST00000391993.7:c.1712+6_1712+8del	ENSP00000375851.3:n.1712+6_1712+8del
ENST00000483951.1:n.258+6_258+8del
NM_001139490.1:c.1712+6_1712+8del	NP_001132962.1:n.1712+6_1712+8del
NM_015650.3:c.1910+6_1910+8del	NP_056465.2:n.1910+6_1910+8del
XM_006712414.1:c.1709+6_1709+8del	XP_006712477.1:n.1709+6_1709+8del
XM_011510944.1:c.2012+6_2012+8del	XP_011509246.1:n.2012+6_2012+8del
XM_011510945.1:c.1973+6_1973+8del	XP_011509247.1:n.1973+6_1973+8del
XM_011510946.1:c.1940+6_1940+8del	XP_011509248.1:n.1940+6_1940+8del
XM_011510947.1:c.1880+6_1880+8del	XP_011509249.1:n.1880+6_1880+8del
XM_011510948.1:c.1814+6_1814+8del	XP_011509250.1:n.1814+6_1814+8del
XM_011510950.1:c.878+6_878+8del	XP_011509252.1:n.878+6_878+8del
XM_006712414.2:c.1709+6_1709+8del	XP_006712477.1:n.1709+6_1709+8del
XM_011510944.2:c.2012+6_2012+8del	XP_011509246.1:n.2012+6_2012+8del
XM_011510945.2:c.1973+6_1973+8del	XP_011509247.1:n.1973+6_1973+8del
XM_011510946.2:c.1940+6_1940+8del	XP_011509248.1:n.1940+6_1940+8del
XM_011510947.2:c.1880+6_1880+8del	XP_011509249.1:n.1880+6_1880+8del
XM_011510948.2:c.1814+6_1814+8del	XP_011509250.1:n.1814+6_1814+8del
XM_011510950.2:c.878+6_878+8del	XP_011509252.1:n.878+6_878+8del
XM_017003789.1:c.2009+6_2009+8del	XP_016859278.1:n.2009+6_2009+8del
XR_001738696.1:n.1738+6_1738+8del
XR_001738697.1:n.1735+6_1735+8del
NM_015650.4:c.1910+6_1910+8del MANE Select	NP_056465.2:n.1910+6_1910+8del