Canonical Allele Identifier: CA2250304826

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948874_16948875delinsGA , CM000679.2:g.16948874_16948875delinsGA	GRCh38
NC_000017.10:g.16852188_16852189delinsGA , CM000679.1:g.16852188_16852189delinsGA	GRCh37
NC_000017.9:g.16792913_16792914delinsGA	NCBI36
NG_007281.1:g.28214_28215delinsTC , LRG_120:g.28214_28215delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.308_309delinsTC MANE Select	ENSP00000261652.2:p.Phe103=
ENST00000261652.6:c.308_309delinsTC	ENSP00000261652.2:p.Phe103=
ENST00000579315.5:c.308_309delinsTC	ENSP00000464069.1:p.Phe103=
ENST00000581616.2:n.311_312delinsTC
ENST00000582931.5:n.212_213delinsTC
ENST00000583789.1:c.170_171delinsTC	ENSP00000462952.1:p.Phe57=
ENST00000584950.5:c.170_171delinsTC	ENSP00000463582.1:p.Phe57=
NM_012452.2:c.308_309delinsTC , LRG_120t1:c.308_309delinsTC	NP_036584.1:p.Phe103=
NM_012452.3:c.308_309delinsTC MANE Select	NP_036584.1:p.Phe103=