Canonical Allele Identifier: CA2036268249
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913979C= , CM000674.2:g.51913979C= GRCh38
NC_000012.11:g.52307763C= , CM000674.1:g.52307763C= GRCh37
NC_000012.10:g.50594030C= NCBI36
NG_009549.1:g.11562C= , LRG_543:g.11562C=

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.356-460C= ENSP00000446724.2:n.356-460C=
ENST00000551576.6:c.531C= ENSP00000455848.2:p.Leu177=
ENST00000552678.2:c.531C= ENSP00000457394.2:p.Leu177=
ENST00000388922.9:c.531C= MANE Select ENSP00000373574.4:p.Leu177=
ENST00000388922.8:c.531C= ENSP00000373574.4:p.Leu177=
ENST00000419526.6:c.104-460C= ENSP00000392492.2:n.104-460C=
ENST00000547400.5:c.356-460C= ENSP00000446724.1:n.356-460C=
ENST00000550683.5:c.573C= ENSP00000447884.1:p.Leu191=
NM_000020.2:c.531C= , LRG_543t1:c.531C= NP_000011.2:p.Leu177=
NM_001077401.1:c.531C= NP_001070869.1:p.Leu177=
XM_005269235.2:c.531C= XP_005269292.1:p.Leu177=
XM_011539008.1:c.356-460C= XP_011537310.1:n.356-460C=
XM_024449279.1:c.-165+209C= XP_024305047.1:n.-165+209C=
NM_000020.3:c.531C= MANE Select NP_000011.2:p.Leu177=
NM_001077401.2:c.531C= NP_001070869.1:p.Leu177=