Canonical Allele Identifier: CA2839276766

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915968C>A , CM000674.2:g.51915968C>A	GRCh38
NC_000012.11:g.52309752C>A , CM000674.1:g.52309752C>A	GRCh37
NC_000012.10:g.50596019C>A	NCBI36
NG_009549.1:g.13551C>A , LRG_543:g.13551C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.779-68C>A	ENSP00000446724.2:n.779-68C>A
ENST00000551576.6:c.1049-68C>A	ENSP00000455848.2:n.1049-68C>A
ENST00000552678.2:c.1049-68C>A	ENSP00000457394.2:n.1049-68C>A
ENST00000388922.9:c.1049-68C>A MANE Select	ENSP00000373574.4:n.1049-68C>A
ENST00000388922.8:c.1049-68C>A	ENSP00000373574.4:n.1049-68C>A
ENST00000419526.6:c.527-68C>A	ENSP00000392492.2:n.527-68C>A
ENST00000547632.1:n.256C>A
ENST00000550683.5:c.1091-68C>A	ENSP00000447884.1:n.1091-68C>A
ENST00000552678.1:c.54-68C>A
NM_000020.2:c.1049-68C>A , LRG_543t1:c.1049-68C>A	NP_000011.2:n.1049-68C>A
NM_001077401.1:c.1049-68C>A	NP_001070869.1:n.1049-68C>A
XM_005269235.2:c.1049-68C>A	XP_005269292.1:n.1049-68C>A
XM_011539008.1:c.779-68C>A	XP_011537310.1:n.779-68C>A
XM_024449279.1:c.260-68C>A	XP_024305047.1:n.260-68C>A
NM_000020.3:c.1049-68C>A MANE Select	NP_000011.2:n.1049-68C>A
NM_001077401.2:c.1049-68C>A	NP_001070869.1:n.1049-68C>A