Canonical Allele Identifier: CA552735320

Gene: ANTXR2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80028675C>G , CM000666.2:g.80028675C>G	GRCh38
NC_000004.11:g.80949829C>G , CM000666.1:g.80949829C>G	GRCh37
NC_000004.10:g.81168853C>G	NCBI36
NG_015987.1:g.49649G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403729.7:c.866+2948G>C MANE Select	ENSP00000385575.2:n.866+2948G>C
ENST00000679571.1:c.635+2948G>C	ENSP00000506307.1:n.635+2948G>C
ENST00000680913.1:c.866+2948G>C	ENSP00000505640.1:n.866+2948G>C
ENST00000681115.1:c.866+2948G>C	ENSP00000505618.1:n.866+2948G>C
ENST00000681710.1:c.635+2948G>C	ENSP00000505865.1:n.635+2948G>C
ENST00000307333.7:c.866+2948G>C	ENSP00000306185.6:n.866+2948G>C
ENST00000346652.10:c.637-20059G>C	ENSP00000314883.6:n.637-20059G>C
ENST00000403729.6:c.866+2948G>C	ENSP00000385575.2:n.866+2948G>C
ENST00000404191.5:c.635+2948G>C	ENSP00000384028.1:n.635+2948G>C
ENST00000449651.5:c.635+2948G>C	ENSP00000413700.1:n.635+2948G>C
NM_001145794.1:c.866+2948G>C	NP_001139266.1:n.866+2948G>C
NM_001286780.1:c.635+2948G>C	NP_001273709.1:n.635+2948G>C
NM_001286781.1:c.635+2948G>C	NP_001273710.1:n.635+2948G>C
NM_058172.5:c.866+2948G>C	NP_477520.2:n.866+2948G>C
XM_011531587.1:c.635+2948G>C	XP_011529889.1:n.635+2948G>C
XM_011531587.3:c.635+2948G>C	XP_011529889.1:n.635+2948G>C
NM_058172.6:c.866+2948G>C MANE Select	NP_477520.2:n.866+2948G>C
NM_001286780.2:c.635+2948G>C	NP_001273709.1:n.635+2948G>C
NM_001286781.2:c.635+2948G>C	NP_001273710.1:n.635+2948G>C
NM_001145794.2:c.866+2948G>C	NP_001139266.1:n.866+2948G>C