Canonical Allele Identifier: CA100504965

Gene: ANTXR2

Linked Data

• dbSNP Id: rs978810130
• MyVariant Identifiers: chr4:g.80993691G>C (hg19) ; chr4:g.80072537G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80072537G>C , CM000666.2:g.80072537G>C	GRCh38
NC_000004.11:g.80993691G>C , CM000666.1:g.80993691G>C	GRCh37
NC_000004.10:g.81212715G>C	NCBI36
NG_015987.1:g.5787C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403729.7:c.24C>G MANE Select	ENSP00000385575.2:p.Ala8=
ENST00000679571.1:c.-80+172C>G	ENSP00000506307.1:n.-80+172C>G
ENST00000680913.1:c.24C>G	ENSP00000505640.1:p.Ala8=
ENST00000681115.1:c.24C>G	ENSP00000505618.1:p.Ala8=
ENST00000681710.1:c.-80+172C>G	ENSP00000505865.1:n.-80+172C>G
ENST00000307333.7:c.24C>G	ENSP00000306185.6:p.Ala8=
ENST00000346652.10:c.24C>G	ENSP00000314883.6:p.Ala8=
ENST00000403729.6:c.24C>G	ENSP00000385575.2:p.Ala8=
ENST00000404191.5:c.-80+858C>G	ENSP00000384028.1:n.-80+858C>G
ENST00000506286.1:n.630-883C>G
ENST00000514959.1:n.248+6816C>G
NM_001145794.1:c.24C>G	NP_001139266.1:p.Ala8=
NM_001286780.1:c.-80+858C>G	NP_001273709.1:n.-80+858C>G
NM_001286781.1:c.-80+172C>G	NP_001273710.1:n.-80+172C>G
NM_058172.5:c.24C>G	NP_477520.2:p.Ala8=
XM_011531587.1:c.-80+858C>G	XP_011529889.1:n.-80+858C>G
XM_011531587.3:c.-80+858C>G	XP_011529889.1:n.-80+858C>G
NM_058172.6:c.24C>G MANE Select	NP_477520.2:p.Ala8=
NM_001286780.2:c.-80+858C>G	NP_001273709.1:n.-80+858C>G
NM_001286781.2:c.-80+172C>G	NP_001273710.1:n.-80+172C>G
NM_001145794.2:c.24C>G	NP_001139266.1:p.Ala8=