Canonical Allele Identifier: CA478504976

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442573G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333407G>A , CM000674.2:g.6333407G>A	GRCh38
NC_000012.11:g.6442573G>A , CM000674.1:g.6442573G>A	GRCh37
NC_000012.10:g.6312834G>A	NCBI36
NG_007506.1:g.13689C>T , LRG_193:g.13689C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.466C>T
ENST00000437813.8:c.432C>T	ENSP00000513672.1:p.Phe144=
ENST00000440083.7:c.432C>T	ENSP00000413224.3:p.Phe144=
ENST00000535958.2:c.*259C>T	ENSP00000513673.1:n.*259C>T
ENST00000698339.1:c.432C>T	ENSP00000513670.1:p.Phe144=
ENST00000698340.1:c.432C>T	ENSP00000513671.1:p.Phe144=
ENST00000162749.7:c.432C>T MANE Select	ENSP00000162749.2:p.Phe144=
ENST00000162749.6:c.432C>T	ENSP00000162749.2:p.Phe144=
ENST00000366159.8:c.432C>T	ENSP00000380389.3:p.Phe144=
ENST00000437813.7:n.393C>T
ENST00000440083.6:c.432C>T	ENSP00000413224.2:p.Phe144=
ENST00000534885.5:c.278C>T	ENSP00000441803.1:p.Ser93Leu
ENST00000537842.5:n.36C>T
ENST00000539372.5:c.432C>T	ENSP00000442059.1:p.Phe144=
ENST00000540022.5:c.303C>T	ENSP00000438343.1:p.Phe101=
ENST00000543048.5:c.*43C>T	ENSP00000439981.1:n.*43C>T
ENST00000543995.5:c.*19C>T	ENSP00000442405.1:n.*19C>T
NM_001065.3:c.432C>T , LRG_193t1:c.432C>T	NP_001056.1:p.Phe144=
NM_001346091.1:c.108C>T	NP_001333020.1:p.Phe36=
NM_001346092.1:c.-146C>T	NP_001333021.1:n.-146C>T
NR_144351.1:n.735C>T
NM_001065.4:c.432C>T MANE Select	NP_001056.1:p.Phe144=
NM_001346091.2:c.108C>T	NP_001333020.1:p.Phe36=
NM_001346092.2:c.-146C>T	NP_001333021.1:n.-146C>T
NR_144351.2:n.694C>T