Canonical Allele Identifier: CA383545896

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439085T>A (hg19) ; chr12:g.6329919T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329919T>A , CM000674.2:g.6329919T>A	GRCh38
NC_000012.11:g.6439085T>A , CM000674.1:g.6439085T>A	GRCh37
NC_000012.10:g.6309346T>A	NCBI36
NG_007506.1:g.17177A>T , LRG_193:g.17177A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2017A>T
ENST00000437813.8:c.*377A>T	ENSP00000513672.1:n.*377A>T
ENST00000440083.7:c.1135A>T	ENSP00000413224.3:p.Asn379Tyr
ENST00000535958.2:c.*743A>T	ENSP00000513673.1:n.*743A>T
ENST00000698337.1:n.877A>T
ENST00000698338.1:n.1530A>T
ENST00000698339.1:c.*411A>T	ENSP00000513670.1:n.*411A>T
ENST00000698340.1:c.*155A>T	ENSP00000513671.1:n.*155A>T
ENST00000162749.7:c.916A>T MANE Select	ENSP00000162749.2:p.Asn306Tyr
ENST00000162749.6:c.916A>T	ENSP00000162749.2:p.Asn306Tyr
ENST00000534885.5:c.*393A>T	ENSP00000441803.1:n.*393A>T
ENST00000536717.5:n.820A>T
ENST00000537842.5:n.373-20A>T
ENST00000540022.5:c.787A>T	ENSP00000438343.1:p.Asn263Tyr
ENST00000543359.5:n.328A>T
ENST00000543995.5:c.*503A>T	ENSP00000442405.1:n.*503A>T
NM_001065.3:c.916A>T , LRG_193t1:c.916A>T	NP_001056.1:p.Asn306Tyr
NM_001346091.1:c.592A>T	NP_001333020.1:p.Asn198Tyr
NM_001346092.1:c.457A>T	NP_001333021.1:p.Asn153Tyr
NR_144351.1:n.1145A>T
NM_001065.4:c.916A>T MANE Select	NP_001056.1:p.Asn306Tyr
NM_001346091.2:c.592A>T	NP_001333020.1:p.Asn198Tyr
NM_001346092.2:c.457A>T	NP_001333021.1:p.Asn153Tyr
NR_144351.2:n.1104A>T