Canonical Allele Identifier: CA383545899

Gene: TNFRSF1A

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2017A>C
ENST00000437813.8:c.*377A>C	ENSP00000513672.1:n.*377A>C
ENST00000440083.7:c.1135A>C	ENSP00000413224.3:p.Asn379His
ENST00000535958.2:c.*743A>C	ENSP00000513673.1:n.*743A>C
ENST00000698337.1:n.877A>C
ENST00000698338.1:n.1530A>C
ENST00000698339.1:c.*411A>C	ENSP00000513670.1:n.*411A>C
ENST00000698340.1:c.*155A>C	ENSP00000513671.1:n.*155A>C
ENST00000162749.7:c.916A>C MANE Select	ENSP00000162749.2:p.Asn306His
ENST00000162749.6:c.916A>C	ENSP00000162749.2:p.Asn306His
ENST00000534885.5:c.*393A>C	ENSP00000441803.1:n.*393A>C
ENST00000536717.5:n.820A>C
ENST00000537842.5:n.373-20A>C
ENST00000540022.5:c.787A>C	ENSP00000438343.1:p.Asn263His
ENST00000543359.5:n.328A>C
ENST00000543995.5:c.*503A>C	ENSP00000442405.1:n.*503A>C
NM_001065.3:c.916A>C , LRG_193t1:c.916A>C	NP_001056.1:p.Asn306His
NM_001346091.1:c.592A>C	NP_001333020.1:p.Asn198His
NM_001346092.1:c.457A>C	NP_001333021.1:p.Asn153His
NR_144351.1:n.1145A>C
NM_001065.4:c.916A>C MANE Select	NP_001056.1:p.Asn306His
NM_001346091.2:c.592A>C	NP_001333020.1:p.Asn198His
NM_001346092.2:c.457A>C	NP_001333021.1:p.Asn153His
NR_144351.2:n.1104A>C