Canonical Allele Identifier: CA798912477

Gene: ANTXR2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.79952008G>T , CM000666.2:g.79952008G>T	GRCh38
NC_000004.11:g.80873162G>T , CM000666.1:g.80873162G>T	GRCh37
NC_000004.10:g.81092186G>T	NCBI36
NG_015987.1:g.126316C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_058172.6:c.1428+25613C>A MANE Select	NP_477520.2:n.1428+25613C>A
ENST00000403729.7:c.1428+25613C>A MANE Select	ENSP00000385575.2:n.1428+25613C>A
NM_001286780.1:c.1197+25613C>A	NP_001273709.1:n.1197+25613C>A
NM_001286780.2:c.1197+25613C>A	NP_001273709.1:n.1197+25613C>A
NM_001286781.1:c.1197+25613C>A	NP_001273710.1:n.1197+25613C>A
NM_001286781.2:c.1197+25613C>A	NP_001273710.1:n.1197+25613C>A
NM_058172.5:c.1428+25613C>A	NP_477520.2:n.1428+25613C>A
ENST00000403729.6:c.1428+25613C>A	ENSP00000385575.2:n.1428+25613C>A
ENST00000404191.5:c.1197+25613C>A	ENSP00000384028.1:n.1197+25613C>A
ENST00000449651.5:c.*578+25613C>A	ENSP00000413700.1:n.*578+25613C>A
ENST00000482406.1:n.226+12657C>A
ENST00000491345.1:n.259+12831C>A
ENST00000679571.1:c.1197+25613C>A	ENSP00000506307.1:n.1197+25613C>A
ENST00000680913.1:c.1428+25613C>A	ENSP00000505640.1:n.1428+25613C>A
ENST00000681115.1:c.1428+25613C>A	ENSP00000505618.1:n.1428+25613C>A
ENST00000681710.1:c.1197+25613C>A	ENSP00000505865.1:n.1197+25613C>A