Canonical Allele Identifier: CA2036269414
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51915216T= , CM000674.2:g.51915216T= GRCh38
NC_000012.11:g.52309000T= , CM000674.1:g.52309000T= GRCh37
NC_000012.10:g.50595267T= NCBI36
NG_009549.1:g.12799T= , LRG_543:g.12799T=

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.503-9T= ENSP00000446724.2:n.503-9T=
ENST00000551576.6:c.773-9T= ENSP00000455848.2:n.773-9T=
ENST00000552678.2:c.773-9T= ENSP00000457394.2:n.773-9T=
ENST00000388922.9:c.773-9T= MANE Select ENSP00000373574.4:n.773-9T=
ENST00000388922.8:c.773-9T= ENSP00000373574.4:n.773-9T=
ENST00000419526.6:c.251-9T= ENSP00000392492.2:n.251-9T=
ENST00000550683.5:c.815-9T= ENSP00000447884.1:n.815-9T=
NM_000020.2:c.773-9T= , LRG_543t1:c.773-9T= NP_000011.2:n.773-9T=
NM_001077401.1:c.773-9T= NP_001070869.1:n.773-9T=
XM_005269235.2:c.773-9T= XP_005269292.1:n.773-9T=
XM_011539008.1:c.503-9T= XP_011537310.1:n.503-9T=
XM_024449279.1:c.-17-9T= XP_024305047.1:n.-17-9T=
NM_000020.3:c.773-9T= MANE Select NP_000011.2:n.773-9T=
NM_001077401.2:c.773-9T= NP_001070869.1:n.773-9T=