Canonical Allele Identifier: CA2036268453
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51914073G= , CM000674.2:g.51914073G= GRCh38
NC_000012.11:g.52307857G= , CM000674.1:g.52307857G= GRCh37
NC_000012.10:g.50594124G= NCBI36
NG_009549.1:g.11656G= , LRG_543:g.11656G=

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.356-366G= ENSP00000446724.2:n.356-366G=
ENST00000551576.6:c.625G= ENSP00000455848.2:p.Gly209=
ENST00000552678.2:c.625G= ENSP00000457394.2:p.Gly209=
ENST00000388922.9:c.625G= MANE Select ENSP00000373574.4:p.Gly209=
ENST00000388922.8:c.625G= ENSP00000373574.4:p.Gly209=
ENST00000419526.6:c.104-366G= ENSP00000392492.2:n.104-366G=
ENST00000547400.5:c.356-366G= ENSP00000446724.1:n.356-366G=
ENST00000550683.5:c.667G= ENSP00000447884.1:p.Gly223=
NM_000020.2:c.625G= , LRG_543t1:c.625G= NP_000011.2:p.Gly209=
NM_001077401.1:c.625G= NP_001070869.1:p.Gly209=
XM_005269235.2:c.625G= XP_005269292.1:p.Gly209=
XM_011539008.1:c.356-366G= XP_011537310.1:n.356-366G=
XM_024449279.1:c.-165+303G= XP_024305047.1:n.-165+303G=
NM_000020.3:c.625G= MANE Select NP_000011.2:p.Gly209=
NM_001077401.2:c.625G= NP_001070869.1:p.Gly209=