Canonical Allele Identifier: CA478505090

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6334191-G-A
• MyVariant Identifiers: chr12:g.6443357G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6334191G>A , CM000674.2:g.6334191G>A	GRCh38
NC_000012.11:g.6443357G>A , CM000674.1:g.6443357G>A	GRCh37
NC_000012.10:g.6313618G>A	NCBI36
NG_007506.1:g.12905C>T , LRG_193:g.12905C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.127C>T
ENST00000437813.8:c.93C>T	ENSP00000513672.1:p.Val31=
ENST00000440083.7:c.93C>T	ENSP00000413224.3:p.Val31=
ENST00000535958.2:c.93C>T	ENSP00000513673.1:p.Val31=
ENST00000698339.1:c.93C>T	ENSP00000513670.1:p.Val31=
ENST00000698340.1:c.93C>T	ENSP00000513671.1:p.Val31=
ENST00000162749.7:c.93C>T MANE Select	ENSP00000162749.2:p.Val31=
ENST00000162749.6:c.93C>T	ENSP00000162749.2:p.Val31=
ENST00000366159.8:c.93C>T	ENSP00000380389.3:p.Val31=
ENST00000437813.7:n.54C>T
ENST00000440083.6:c.93C>T	ENSP00000413224.2:p.Val31=
ENST00000534885.5:c.40-326C>T	ENSP00000441803.1:n.40-326C>T
ENST00000535958.1:n.314C>T
ENST00000536194.1:c.93C>T	ENSP00000442919.1:p.Val31=
ENST00000538363.1:n.283C>T
ENST00000539372.5:c.93C>T	ENSP00000442059.1:p.Val31=
ENST00000540022.5:c.93C>T	ENSP00000438343.1:p.Val31=
ENST00000543048.5:c.93C>T	ENSP00000439981.1:p.Val31=
ENST00000543995.5:c.93C>T	ENSP00000442405.1:p.Val31=
NM_001065.3:c.93C>T , LRG_193t1:c.93C>T	NP_001056.1:p.Val31=
NM_001346091.1:c.-131-326C>T	NP_001333020.1:n.-131-326C>T
NM_001346092.1:c.-485C>T	NP_001333021.1:n.-485C>T
NR_144351.1:n.396C>T
NM_001065.4:c.93C>T MANE Select	NP_001056.1:p.Val31=
NM_001346091.2:c.-131-326C>T	NP_001333020.1:n.-131-326C>T
NM_001346092.2:c.-485C>T	NP_001333021.1:n.-485C>T
NR_144351.2:n.355C>T