Canonical Allele Identifier: CA2813445886

Gene: TNFSF14

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6670073_6670074insCCCCCAAACACACCCAACAC , CM000681.2:g.6670073_6670074insCCCCCAAACACACCCAACAC	GRCh38
NC_000019.9:g.6670084_6670085insCCCCCAAACACACCCAACAC , CM000681.1:g.6670084_6670085insCCCCCAAACACACCCAACAC	GRCh37
NC_000019.8:g.6621084_6621085insCCCCCAAACACACCCAACAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675206.1:c.-4_-3insTGTTGGGTGTGTTTGGGGGG MANE Select	ENSP00000502837.1:n.-4_-3insTGTTGGGTGTGTTTGGGGGG
ENST00000245912.7:c.-4_-3insTGTTGGGTGTGTTTGGGGGG	ENSP00000245912.3:n.-4_-3insTGTTGGGTGTGTTTGGGGGG
ENST00000599359.1:c.-4_-3insTGTTGGGTGTGTTTGGGGGG	ENSP00000469049.1:n.-4_-3insTGTTGGGTGTGTTTGGGGGG
NM_003807.3:c.-4_-3insTGTTGGGTGTGTTTGGGGGG	NP_003798.2:n.-4_-3insTGTTGGGTGTGTTTGGGGGG
NM_172014.2:c.-4_-3insTGTTGGGTGTGTTTGGGGGG	NP_742011.2:n.-4_-3insTGTTGGGTGTGTTTGGGGGG
XM_005259670.2:c.-4_-3insTGTTGGGTGTGTTTGGGGGG	XP_005259727.1:n.-4_-3insTGTTGGGTGTGTTTGGGGGG
XM_011528398.1:c.-4_-3insTGTTGGGTGTGTTTGGGGGG	XP_011526700.1:n.-4_-3insTGTTGGGTGTGTTTGGGGGG
XR_936212.1:n.511_512insTGTTGGGTGTGTTTGGGGGG
NM_003807.4:c.-4_-3insTGTTGGGTGTGTTTGGGGGG	NP_003798.2:n.-4_-3insTGTTGGGTGTGTTTGGGGGG
NM_172014.3:c.-4_-3insTGTTGGGTGTGTTTGGGGGG	NP_742011.2:n.-4_-3insTGTTGGGTGTGTTTGGGGGG
XM_017027417.1:c.-4_-3insTGTTGGGTGTGTTTGGGGGG	XP_016882906.1:n.-4_-3insTGTTGGGTGTGTTTGGGGGG
XM_017027418.1:c.-4_-3insTGTTGGGTGTGTTTGGGGGG	XP_016882907.1:n.-4_-3insTGTTGGGTGTGTTTGGGGGG
XR_001753777.1:n.523_524insTGTTGGGTGTGTTTGGGGGG
XR_936212.2:n.523_524insTGTTGGGTGTGTTTGGGGGG
NM_001376887.1:c.-4_-3insTGTTGGGTGTGTTTGGGGGG MANE Select	NP_001363816.1:n.-4_-3insTGTTGGGTGTGTTTGGGGGG
NM_003807.5:c.-4_-3insTGTTGGGTGTGTTTGGGGGG	NP_003798.2:n.-4_-3insTGTTGGGTGTGTTTGGGGGG