Canonical Allele Identifier: CA2320545643

Gene: TNFSF14

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6669791C= , CM000681.2:g.6669791C=	GRCh38
NC_000019.9:g.6669802C= , CM000681.1:g.6669802C=	GRCh37
NC_000019.8:g.6620802C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000675206.1:c.219+60G= MANE Select	ENSP00000502837.1:n.219+60G=
ENST00000245912.7:c.111+168G=	ENSP00000245912.3:n.111+168G=
ENST00000599359.1:c.219+60G=	ENSP00000469049.1:n.219+60G=
NM_003807.3:c.219+60G=	NP_003798.2:n.219+60G=
NM_172014.2:c.111+168G=	NP_742011.2:n.111+168G=
XM_005259670.2:c.111+168G=	XP_005259727.1:n.111+168G=
XM_011528398.1:c.253+26G=	XP_011526700.1:n.253+26G=
XR_936212.1:n.733+60G=
NM_003807.4:c.219+60G=	NP_003798.2:n.219+60G=
NM_172014.3:c.111+168G=	NP_742011.2:n.111+168G=
XM_017027417.1:c.219+60G=	XP_016882906.1:n.219+60G=
XM_017027418.1:c.219+60G=	XP_016882907.1:n.219+60G=
XR_001753777.1:n.745+60G=
XR_936212.2:n.745+60G=
NM_001376887.1:c.219+60G= MANE Select	NP_001363816.1:n.219+60G=
NM_003807.5:c.219+60G=	NP_003798.2:n.219+60G=