Canonical Allele Identifier: CA2036269461
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51915323A= , CM000674.2:g.51915323A= GRCh38
NC_000012.11:g.52309107A= , CM000674.1:g.52309107A= GRCh37
NC_000012.10:g.50595374A= NCBI36
NG_009549.1:g.12906A= , LRG_543:g.12906A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.601A= ENSP00000446724.2:p.Arg201=
ENST00000551576.6:c.871A= ENSP00000455848.2:p.Arg291=
ENST00000552678.2:c.871A= ENSP00000457394.2:p.Arg291=
ENST00000388922.9:c.871A= MANE Select ENSP00000373574.4:p.Arg291=
ENST00000388922.8:c.871A= ENSP00000373574.4:p.Arg291=
ENST00000419526.6:c.349A= ENSP00000392492.2:p.Arg117=
ENST00000550683.5:c.913A= ENSP00000447884.1:p.Arg305=
NM_000020.2:c.871A= , LRG_543t1:c.871A= NP_000011.2:p.Arg291=
NM_001077401.1:c.871A= NP_001070869.1:p.Arg291=
XM_005269235.2:c.871A= XP_005269292.1:p.Arg291=
XM_011539008.1:c.601A= XP_011537310.1:p.Arg201=
XM_024449279.1:c.82A= XP_024305047.1:p.Arg28=
NM_000020.3:c.871A= MANE Select NP_000011.2:p.Arg291=
NM_001077401.2:c.871A= NP_001070869.1:p.Arg291=