Canonical Allele Identifier: CA1296491976

Gene: ACVR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.147854458C= , CM000664.2:g.147854458C=	GRCh38
NC_000002.11:g.148612027C= , CM000664.1:g.148612027C=	GRCh37
NC_000002.10:g.148328497C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241416.12:c.55+9251C= MANE Select	ENSP00000241416.7:n.55+9251C=
ENST00000241416.11:c.55+9251C=	ENSP00000241416.7:n.55+9251C=
ENST00000404590.1:c.55+9251C=	ENSP00000384338.1:n.55+9251C=
ENST00000462659.1:n.183+9752C=
ENST00000465329.1:n.179+9251C=
ENST00000487959.5:n.190+9752C=
ENST00000535787.5:c.-207+9752C=	ENSP00000439988.1:n.-207+9752C=
NM_001278579.1:c.55+9251C=	NP_001265508.1:n.55+9251C=
NM_001278580.1:c.-207+9752C=	NP_001265509.1:n.-207+9752C=
NM_001616.4:c.55+9251C=	NP_001607.1:n.55+9251C=
XM_005263843.2:c.55+9251C=	XP_005263900.1:n.55+9251C=
NM_001616.5:c.55+9251C= MANE Select	NP_001607.1:n.55+9251C=
NM_001278579.2:c.55+9251C=	NP_001265508.1:n.55+9251C=
NM_001278580.2:c.-207+9752C=	NP_001265509.1:n.-207+9752C=