Canonical Allele Identifier: CA478504989

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6333771-G-T
• MyVariant Identifiers: chr12:g.6442937G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333771G>T , CM000674.2:g.6333771G>T	GRCh38
NC_000012.11:g.6442937G>T , CM000674.1:g.6442937G>T	GRCh37
NC_000012.10:g.6313198G>T	NCBI36
NG_007506.1:g.13325C>A , LRG_193:g.13325C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.322C>A
ENST00000437813.8:c.288C>A	ENSP00000513672.1:p.Leu96=
ENST00000440083.7:c.288C>A	ENSP00000413224.3:p.Leu96=
ENST00000535958.2:c.*115C>A	ENSP00000513673.1:n.*115C>A
ENST00000698339.1:c.288C>A	ENSP00000513670.1:p.Leu96=
ENST00000698340.1:c.288C>A	ENSP00000513671.1:p.Leu96=
ENST00000162749.7:c.288C>A MANE Select	ENSP00000162749.2:p.Leu96=
ENST00000162749.6:c.288C>A	ENSP00000162749.2:p.Leu96=
ENST00000366159.8:c.288C>A	ENSP00000380389.3:p.Leu96=
ENST00000437813.7:n.249C>A
ENST00000440083.6:c.288C>A	ENSP00000413224.2:p.Leu96=
ENST00000534885.5:c.134C>A	ENSP00000441803.1:p.Ser45Ter
ENST00000535958.1:n.534C>A
ENST00000536194.1:c.261C>A	ENSP00000442919.1:p.Leu87=
ENST00000539372.5:c.288C>A	ENSP00000442059.1:p.Leu96=
ENST00000540022.5:c.194-255C>A	ENSP00000438343.1:n.194-255C>A
ENST00000543048.5:c.214+74C>A	ENSP00000439981.1:n.214+74C>A
ENST00000543995.5:c.194-320C>A	ENSP00000442405.1:n.194-320C>A
NM_001065.3:c.288C>A , LRG_193t1:c.288C>A	NP_001056.1:p.Leu96=
NM_001346091.1:c.-37C>A	NP_001333020.1:n.-37C>A
NM_001346092.1:c.-290C>A	NP_001333021.1:n.-290C>A
NR_144351.1:n.591C>A
NM_001065.4:c.288C>A MANE Select	NP_001056.1:p.Leu96=
NM_001346091.2:c.-37C>A	NP_001333020.1:n.-37C>A
NM_001346092.2:c.-290C>A	NP_001333021.1:n.-290C>A
NR_144351.2:n.550C>A