Canonical Allele Identifier: CA2014026225
Gene: TNFRSF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6333763_6333766delinsCAGT , CM000674.2:g.6333763_6333766delinsCAGT GRCh38
NC_000012.11:g.6442929_6442932delinsCAGT , CM000674.1:g.6442929_6442932delinsCAGT GRCh37
NC_000012.10:g.6313190_6313193delinsCAGT NCBI36
NG_007506.1:g.13330_13333delinsACTG , LRG_193:g.13330_13333delinsACTG

Transcript Alleles

HGVS Amino-acid change
ENST00000366159.9:n.327_330delinsACTG
ENST00000437813.8:c.293_296delinsACTG ENSP00000513672.1:p.His98=
ENST00000440083.7:c.293_296delinsACTG ENSP00000413224.3:p.His98=
ENST00000535958.2:c.*120_*123delinsACTG ENSP00000513673.1:n.*120_*123delinsACTG
ENST00000698339.1:c.293_296delinsACTG ENSP00000513670.1:p.His98=
ENST00000698340.1:c.293_296delinsACTG ENSP00000513671.1:p.His98=
ENST00000162749.7:c.293_296delinsACTG MANE Select ENSP00000162749.2:p.His98=
ENST00000162749.6:c.293_296delinsACTG ENSP00000162749.2:p.His98=
ENST00000366159.8:c.293_296delinsACTG ENSP00000380389.3:p.His98=
ENST00000437813.7:n.254_257delinsACTG
ENST00000440083.6:c.293_296delinsACTG ENSP00000413224.2:p.His98=
ENST00000534885.5:c.139_142delinsACTG ENSP00000441803.1:p.Thr47=
ENST00000535958.1:n.539_542delinsACTG
ENST00000536194.1:c.266_269delinsACTG ENSP00000442919.1:p.His89=
ENST00000539372.5:c.293_296delinsACTG ENSP00000442059.1:p.His98=
ENST00000540022.5:c.194-250_194-247delinsACTG ENSP00000438343.1:n.194-250_194-247delins...
ENST00000543048.5:c.214+79_214+82delinsACTG ENSP00000439981.1:n.214+79_214+82delinsAC...
ENST00000543995.5:c.194-315_194-312delinsACTG ENSP00000442405.1:n.194-315_194-312delins...
NM_001065.3:c.293_296delinsACTG , LRG_193t1:c.293_296delinsACTG NP_001056.1:p.His98=
NM_001346091.1:c.-32_-29delinsACTG NP_001333020.1:n.-32_-29delinsACTG
NM_001346092.1:c.-285_-282delinsACTG NP_001333021.1:n.-285_-282delinsACTG
NR_144351.1:n.596_599delinsACTG
NM_001065.4:c.293_296delinsACTG MANE Select NP_001056.1:p.His98=
NM_001346091.2:c.-32_-29delinsACTG NP_001333020.1:n.-32_-29delinsACTG
NM_001346092.2:c.-285_-282delinsACTG NP_001333021.1:n.-285_-282delinsACTG
NR_144351.2:n.555_558delinsACTG