Canonical Allele Identifier: CA2036269510
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51915406C= , CM000674.2:g.51915406C= GRCh38
NC_000012.11:g.52309190C= , CM000674.1:g.52309190C= GRCh37
NC_000012.10:g.50595457C= NCBI36
NG_009549.1:g.12989C= , LRG_543:g.12989C=

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.684C= ENSP00000446724.2:p.Phe228=
ENST00000551576.6:c.954C= ENSP00000455848.2:p.Phe318=
ENST00000552678.2:c.954C= ENSP00000457394.2:p.Phe318=
ENST00000388922.9:c.954C= MANE Select ENSP00000373574.4:p.Phe318=
ENST00000388922.8:c.954C= ENSP00000373574.4:p.Phe318=
ENST00000419526.6:c.432C= ENSP00000392492.2:p.Phe144=
ENST00000550683.5:c.996C= ENSP00000447884.1:p.Phe332=
NM_000020.2:c.954C= , LRG_543t1:c.954C= NP_000011.2:p.Phe318=
NM_001077401.1:c.954C= NP_001070869.1:p.Phe318=
XM_005269235.2:c.954C= XP_005269292.1:p.Phe318=
XM_011539008.1:c.684C= XP_011537310.1:p.Phe228=
XM_024449279.1:c.165C= XP_024305047.1:p.Phe55=
NM_000020.3:c.954C= MANE Select NP_000011.2:p.Phe318=
NM_001077401.2:c.954C= NP_001070869.1:p.Phe318=