Canonical Allele Identifier: CA1207653968

Gene: TNFSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173206720_173206721delinsCA , CM000663.2:g.173206720_173206721delinsCA	GRCh38
NC_000001.10:g.173175859_173175860delinsCA , CM000663.1:g.173175859_173175860delinsCA	GRCh37
NC_000001.9:g.171442482_171442483delinsCA	NCBI36
NG_011477.1:g.5612_5613delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281834.4:c.153+303_153+304delinsTG MANE Select	ENSP00000281834.3:n.153+303_153+304delinsTG
ENST00000281834.3:c.153+303_153+304delinsTG	ENSP00000281834.3:n.153+303_153+304delinsTG
NM_003326.4:c.153+303_153+304delinsTG	NP_003317.1:n.153+303_153+304delinsTG
XM_011509964.1:c.225+303_225+304delinsTG	XP_011508266.1:n.225+303_225+304delinsTG
XM_011509964.2:c.441+303_441+304delinsTG	XP_011508266.2:n.441+303_441+304delinsTG
XM_017002228.1:c.-986_-985delinsTG	XP_016857717.1:n.-986_-985delinsTG
XM_017002229.1:c.186+303_186+304delinsTG	XP_016857718.1:n.186+303_186+304delinsTG
XM_017002230.1:c.180+303_180+304delinsTG	XP_016857719.1:n.180+303_180+304delinsTG
NM_003326.5:c.153+303_153+304delinsTG MANE Select	NP_003317.1:n.153+303_153+304delinsTG