Canonical Allele Identifier: CA2036268866
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51914405G= , CM000674.2:g.51914405G= GRCh38
NC_000012.11:g.52308189G= , CM000674.1:g.52308189G= GRCh37
NC_000012.10:g.50594456G= NCBI36
NG_009549.1:g.11988G= , LRG_543:g.11988G=

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.356-34G= ENSP00000446724.2:n.356-34G=
ENST00000551576.6:c.626-34G= ENSP00000455848.2:n.626-34G=
ENST00000552678.2:c.626-34G= ENSP00000457394.2:n.626-34G=
ENST00000388922.9:c.626-34G= MANE Select ENSP00000373574.4:n.626-34G=
ENST00000388922.8:c.626-34G= ENSP00000373574.4:n.626-34G=
ENST00000419526.6:c.104-34G= ENSP00000392492.2:n.104-34G=
ENST00000547400.5:c.356-34G= ENSP00000446724.1:n.356-34G=
ENST00000550683.5:c.668-34G= ENSP00000447884.1:n.668-34G=
NM_000020.2:c.626-34G= , LRG_543t1:c.626-34G= NP_000011.2:n.626-34G=
NM_001077401.1:c.626-34G= NP_001070869.1:n.626-34G=
XM_005269235.2:c.626-34G= XP_005269292.1:n.626-34G=
XM_011539008.1:c.356-34G= XP_011537310.1:n.356-34G=
XM_024449279.1:c.-164-34G= XP_024305047.1:n.-164-34G=
NM_000020.3:c.626-34G= MANE Select NP_000011.2:n.626-34G=
NM_001077401.2:c.626-34G= NP_001070869.1:n.626-34G=