Canonical Allele Identifier: CA2981740

Gene: ANTXR2

Linked Data

• ClinVar Variation Id: 349875
• ClinVar RCV Id: RCV000339610 ; RCV000904059
• dbSNP Id: rs72653288
• ExAC: 4:80905991 G / C
• gnomAD v2: 4-80905991-G-C
• gnomAD v3: 4-79984837-G-C
• gnomAD v4: 4-79984837-G-C
• MyVariant Identifiers: chr4:g.80905991G>C (hg19) ; chr4:g.79984837G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.79984837G>C , CM000666.2:g.79984837G>C	GRCh38
NC_000004.11:g.80905991G>C , CM000666.1:g.80905991G>C	GRCh37
NC_000004.10:g.81125015G>C	NCBI36
NG_015987.1:g.93487C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403729.7:c.1068C>G MANE Select	ENSP00000385575.2:p.Pro356=
ENST00000679571.1:c.837C>G	ENSP00000506307.1:p.Pro279=
ENST00000680913.1:c.1068C>G	ENSP00000505640.1:p.Pro356=
ENST00000681115.1:c.1068C>G	ENSP00000505618.1:p.Pro356=
ENST00000681710.1:c.837C>G	ENSP00000505865.1:p.Pro279=
ENST00000307333.7:c.1068C>G	ENSP00000306185.6:p.Pro356=
ENST00000346652.10:c.759C>G	ENSP00000314883.6:p.Pro253=
ENST00000403729.6:c.1068C>G	ENSP00000385575.2:p.Pro356=
ENST00000404191.5:c.837C>G	ENSP00000384028.1:p.Pro279=
ENST00000449651.5:c.*218C>G	ENSP00000413700.1:n.*218C>G
NM_001145794.1:c.1068C>G	NP_001139266.1:p.Pro356=
NM_001286780.1:c.837C>G	NP_001273709.1:p.Pro279=
NM_001286781.1:c.837C>G	NP_001273710.1:p.Pro279=
NM_058172.5:c.1068C>G	NP_477520.2:p.Pro356=
XM_011531587.1:c.837C>G	XP_011529889.1:p.Pro279=
XM_011531587.3:c.837C>G	XP_011529889.1:p.Pro279=
NM_058172.6:c.1068C>G MANE Select	NP_477520.2:p.Pro356=
NM_001286780.2:c.837C>G	NP_001273709.1:p.Pro279=
NM_001286781.2:c.837C>G	NP_001273710.1:p.Pro279=
NM_001145794.2:c.1068C>G	NP_001139266.1:p.Pro356=