Canonical Allele Identifier: CA2250305282

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948985_16948986delinsTG , CM000679.2:g.16948985_16948986delinsTG	GRCh38
NC_000017.10:g.16852299_16852300delinsTG , CM000679.1:g.16852299_16852300delinsTG	GRCh37
NC_000017.9:g.16793024_16793025delinsTG	NCBI36
NG_007281.1:g.28103_28104delinsCA , LRG_120:g.28103_28104delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.200-3_200-2delinsCA MANE Select	ENSP00000261652.2:n.200-3_200-2delinsCA
ENST00000261652.6:c.200-3_200-2delinsCA	ENSP00000261652.2:n.200-3_200-2delinsCA
ENST00000579315.5:c.200-3_200-2delinsCA	ENSP00000464069.1:n.200-3_200-2delinsCA
ENST00000581616.2:n.203-3_203-2delinsCA
ENST00000582931.5:n.104-3_104-2delinsCA
ENST00000583789.1:c.62-3_62-2delinsCA	ENSP00000462952.1:n.62-3_62-2delinsCA
ENST00000584950.5:c.62-3_62-2delinsCA	ENSP00000463582.1:n.62-3_62-2delinsCA
NM_012452.2:c.200-3_200-2delinsCA , LRG_120t1:c.200-3_200-2delinsCA	NP_036584.1:n.200-3_200-2delinsCA
NM_012452.3:c.200-3_200-2delinsCA MANE Select	NP_036584.1:n.200-3_200-2delinsCA