Canonical Allele Identifier: CA1296505591

Gene: ACVR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.147885549C= , CM000664.2:g.147885549C=	GRCh38
NC_000002.11:g.148643118C= , CM000664.1:g.148643118C=	GRCh37
NC_000002.10:g.148359588C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241416.12:c.56-10752C= MANE Select	ENSP00000241416.7:n.56-10752C=
ENST00000241416.11:c.56-10752C=	ENSP00000241416.7:n.56-10752C=
ENST00000404590.1:c.56-10752C=	ENSP00000384338.1:n.56-10752C=
ENST00000462659.1:n.184-10752C=
ENST00000465329.1:n.180-10752C=
ENST00000487959.5:n.191-10815C=
ENST00000535787.5:c.-206-10815C=	ENSP00000439988.1:n.-206-10815C=
NM_001278579.1:c.56-10752C=	NP_001265508.1:n.56-10752C=
NM_001278580.1:c.-206-10815C=	NP_001265509.1:n.-206-10815C=
NM_001616.4:c.56-10752C=	NP_001607.1:n.56-10752C=
XM_005263843.2:c.56-10752C=	XP_005263900.1:n.56-10752C=
XR_923436.1:n.301+14881G=
NM_001616.5:c.56-10752C= MANE Select	NP_001607.1:n.56-10752C=
NM_001278579.2:c.56-10752C=	NP_001265508.1:n.56-10752C=
NM_001278580.2:c.-206-10815C=	NP_001265509.1:n.-206-10815C=