Canonical Allele Identifier: CA1296508551

Gene: ACVR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.147891817G= , CM000664.2:g.147891817G=	GRCh38
NC_000002.11:g.148649386G= , CM000664.1:g.148649386G=	GRCh37
NC_000002.10:g.148365856G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001616.5:c.56-4484G= MANE Select	NP_001607.1:n.56-4484G=
ENST00000241416.12:c.56-4484G= MANE Select	ENSP00000241416.7:n.56-4484G=
NM_001278579.1:c.56-4484G=	NP_001265508.1:n.56-4484G=
NM_001278579.2:c.56-4484G=	NP_001265508.1:n.56-4484G=
NM_001278580.1:c.-206-4547G=	NP_001265509.1:n.-206-4547G=
NM_001278580.2:c.-206-4547G=	NP_001265509.1:n.-206-4547G=
NM_001616.4:c.56-4484G=	NP_001607.1:n.56-4484G=
ENST00000241416.11:c.56-4484G=	ENSP00000241416.7:n.56-4484G=
ENST00000404590.1:c.56-4484G=	ENSP00000384338.1:n.56-4484G=
ENST00000462659.1:n.184-4484G=
ENST00000465329.1:n.180-4484G=
ENST00000487959.5:n.191-4547G=
ENST00000535787.5:c.-206-4547G=	ENSP00000439988.1:n.-206-4547G=
XM_005263843.2:c.56-4484G=	XP_005263900.1:n.56-4484G=
XR_923436.1:n.301+8613C=