Canonical Allele Identifier: CA351246492

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306252G>C (hg19) ; chr2:g.238397611G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397611G>C , CM000664.2:g.238397611G>C	GRCh38
NC_000002.11:g.239306252G>C , CM000664.1:g.239306252G>C	GRCh37
NC_000002.10:g.238970991G>C	NCBI36
NG_053055.1:g.82123G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1842G>C MANE Select	ENSP00000362424.4:p.Met614Ile
ENST00000373327.4:c.1842G>C	ENSP00000362424.4:p.Met614Ile
ENST00000391993.7:c.1644G>C	ENSP00000375851.3:p.Met548Ile
ENST00000462122.1:n.853G>C
ENST00000483951.1:n.190G>C
NM_001139490.1:c.1644G>C	NP_001132962.1:p.Met548Ile
NM_015650.3:c.1842G>C	NP_056465.2:p.Met614Ile
XM_006712414.1:c.1641G>C	XP_006712477.1:p.Met547Ile
XM_011510944.1:c.1944G>C	XP_011509246.1:p.Met648Ile
XM_011510945.1:c.1905G>C	XP_011509247.1:p.Met635Ile
XM_011510946.1:c.1872G>C	XP_011509248.1:p.Met624Ile
XM_011510947.1:c.1812G>C	XP_011509249.1:p.Met604Ile
XM_011510948.1:c.1746G>C	XP_011509250.1:p.Met582Ile
XM_011510950.1:c.810G>C	XP_011509252.1:p.Met270Ile
XM_006712414.2:c.1641G>C	XP_006712477.1:p.Met547Ile
XM_011510944.2:c.1944G>C	XP_011509246.1:p.Met648Ile
XM_011510945.2:c.1905G>C	XP_011509247.1:p.Met635Ile
XM_011510946.2:c.1872G>C	XP_011509248.1:p.Met624Ile
XM_011510947.2:c.1812G>C	XP_011509249.1:p.Met604Ile
XM_011510948.2:c.1746G>C	XP_011509250.1:p.Met582Ile
XM_011510950.2:c.810G>C	XP_011509252.1:p.Met270Ile
XM_017003789.1:c.1941G>C	XP_016859278.1:p.Met647Ile
XR_001738696.1:n.1670G>C
XR_001738697.1:n.1667G>C
NM_015650.4:c.1842G>C MANE Select	NP_056465.2:p.Met614Ile