Canonical Allele Identifier: CA891275050

Gene: TNFSF4

Linked Data

• dbSNP Id: rs1170538792
• MyVariant Identifiers: chr1:g.173170556_173170557insGT (hg19) ; chr1:g.173201417_173201418insGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173201426_173201427dup , CM000663.2:g.173201426_173201427dup	GRCh38
NC_000001.10:g.173170565_173170566dup , CM000663.1:g.173170565_173170566dup	GRCh37
NC_000001.9:g.171437188_171437189dup	NCBI36
NG_011477.1:g.10914_10915dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000281834.4:c.153+5605_153+5606dup MANE Select	ENSP00000281834.3:n.153+5605_153+5606dup
ENST00000281834.3:c.153+5605_153+5606dup	ENSP00000281834.3:n.153+5605_153+5606dup
ENST00000367718.5:c.3+3892_3+3893dup	ENSP00000356691.1:n.3+3892_3+3893dup
ENST00000488053.1:n.414+3892_414+3893dup
NM_001297562.1:c.3+3892_3+3893dup	NP_001284491.1:n.3+3892_3+3893dup
NM_003326.4:c.153+5605_153+5606dup	NP_003317.1:n.153+5605_153+5606dup
XM_011509964.1:c.225+5605_225+5606dup	XP_011508266.1:n.225+5605_225+5606dup
XM_011509964.2:c.441+5605_441+5606dup	XP_011508266.2:n.441+5605_441+5606dup
XM_017002228.1:c.249+4068_249+4069dup	XP_016857717.1:n.249+4068_249+4069dup
XM_017002229.1:c.186+5605_186+5606dup	XP_016857718.1:n.186+5605_186+5606dup
XM_017002230.1:c.180+5605_180+5606dup	XP_016857719.1:n.180+5605_180+5606dup
NM_003326.5:c.153+5605_153+5606dup MANE Select	NP_003317.1:n.153+5605_153+5606dup
NM_001297562.2:c.3+3892_3+3893dup	NP_001284491.1:n.3+3892_3+3893dup