Canonical Allele Identifier: CA11086083

Gene: ACVR2A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.147914451C>T , CM000664.2:g.147914451C>T	GRCh38
NC_000002.11:g.148672020C>T , CM000664.1:g.148672020C>T	GRCh37
NC_000002.10:g.148388490C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241416.12:c.529-740C>T MANE Select	ENSP00000241416.7:n.529-740C>T
ENST00000241416.11:c.529-740C>T	ENSP00000241416.7:n.529-740C>T
ENST00000404590.1:c.529-740C>T	ENSP00000384338.1:n.529-740C>T
ENST00000535787.5:c.205-740C>T	ENSP00000439988.1:n.205-740C>T
NM_001278579.1:c.529-740C>T	NP_001265508.1:n.529-740C>T
NM_001278580.1:c.205-740C>T	NP_001265509.1:n.205-740C>T
NM_001616.4:c.529-740C>T	NP_001607.1:n.529-740C>T
XM_005263843.2:c.529-740C>T	XP_005263900.1:n.529-740C>T
NM_001616.5:c.529-740C>T MANE Select	NP_001607.1:n.529-740C>T
NM_001278579.2:c.529-740C>T	NP_001265508.1:n.529-740C>T
NM_001278580.2:c.205-740C>T	NP_001265509.1:n.205-740C>T