Canonical Allele Identifier: CA2078774943

Gene: TNFRSF19

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23631056A= , CM000675.2:g.23631056A=	GRCh38
NC_000013.10:g.24205195A= , CM000675.1:g.24205195A=	GRCh37
NC_000013.9:g.23103195A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_148957.4:c.445+4264A= MANE Select	NP_683760.1:n.445+4264A=
ENST00000248484.9:c.445+4264A= MANE Select	ENSP00000248484.4:n.445+4264A=
NM_001204458.1:c.445+4264A=	NP_001191387.1:n.445+4264A=
NM_001204458.2:c.445+4264A=	NP_001191387.1:n.445+4264A=
NM_001204458.3:c.445+4264A=	NP_001191387.1:n.445+4264A=
NM_001204459.1:c.49+4264A=	NP_001191388.1:n.49+4264A=
NM_001204459.2:c.49+4264A=	NP_001191388.1:n.49+4264A=
NM_001354985.1:c.445+4264A=	NP_001341914.1:n.445+4264A=
NM_001354985.2:c.445+4264A=	NP_001341914.1:n.445+4264A=
NM_018647.3:c.445+4264A=	NP_061117.2:n.445+4264A=
NM_018647.4:c.445+4264A=	NP_061117.2:n.445+4264A=
NM_018647.5:c.445+4264A=	NP_061117.2:n.445+4264A=
NM_148957.3:c.445+4264A=	NP_683760.1:n.445+4264A=
ENST00000248484.8:c.445+4264A=	ENSP00000248484.4:n.445+4264A=
ENST00000382258.8:c.445+4264A=	ENSP00000371693.4:n.445+4264A=
ENST00000382263.3:c.445+4264A=	ENSP00000371698.3:n.445+4264A=
ENST00000403372.6:c.49+4264A=	ENSP00000385408.2:n.49+4264A=
XM_005266445.2:c.445+4264A=	XP_005266502.1:n.445+4264A=
XM_005266445.3:c.445+4264A=	XP_005266502.1:n.445+4264A=
XM_005266446.1:c.445+4264A=	XP_005266503.1:n.445+4264A=
XM_005266446.2:c.445+4264A=	XP_005266503.1:n.445+4264A=
XM_011535146.1:c.445+4264A=	XP_011533448.1:n.445+4264A=
XM_017020651.1:c.445+4264A=	XP_016876140.1:n.445+4264A=