Canonical Allele Identifier: CA383550030

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442590T>A (hg19) ; chr12:g.6333424T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333424T>A , CM000674.2:g.6333424T>A	GRCh38
NC_000012.11:g.6442590T>A , CM000674.1:g.6442590T>A	GRCh37
NC_000012.10:g.6312851T>A	NCBI36
NG_007506.1:g.13672A>T , LRG_193:g.13672A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.449A>T
ENST00000437813.8:c.415A>T	ENSP00000513672.1:p.Asn139Tyr
ENST00000440083.7:c.415A>T	ENSP00000413224.3:p.Asn139Tyr
ENST00000535958.2:c.*242A>T	ENSP00000513673.1:n.*242A>T
ENST00000698339.1:c.415A>T	ENSP00000513670.1:p.Asn139Tyr
ENST00000698340.1:c.415A>T	ENSP00000513671.1:p.Asn139Tyr
ENST00000162749.7:c.415A>T MANE Select	ENSP00000162749.2:p.Asn139Tyr
ENST00000162749.6:c.415A>T	ENSP00000162749.2:p.Asn139Tyr
ENST00000366159.8:c.415A>T	ENSP00000380389.3:p.Asn139Tyr
ENST00000437813.7:n.376A>T
ENST00000440083.6:c.415A>T	ENSP00000413224.2:p.Asn139Tyr
ENST00000534885.5:c.261A>T	ENSP00000441803.1:p.Lys87Asn
ENST00000537842.5:n.19A>T
ENST00000539372.5:c.415A>T	ENSP00000442059.1:p.Asn139Tyr
ENST00000540022.5:c.286A>T	ENSP00000438343.1:p.Asn96Tyr
ENST00000543048.5:c.*26A>T	ENSP00000439981.1:n.*26A>T
ENST00000543995.5:c.*2A>T	ENSP00000442405.1:n.*2A>T
NM_001065.3:c.415A>T , LRG_193t1:c.415A>T	NP_001056.1:p.Asn139Tyr
NM_001346091.1:c.91A>T	NP_001333020.1:p.Asn31Tyr
NM_001346092.1:c.-163A>T	NP_001333021.1:n.-163A>T
NR_144351.1:n.718A>T
NM_001065.4:c.415A>T MANE Select	NP_001056.1:p.Asn139Tyr
NM_001346091.2:c.91A>T	NP_001333020.1:p.Asn31Tyr
NM_001346092.2:c.-163A>T	NP_001333021.1:n.-163A>T
NR_144351.2:n.677A>T