Canonical Allele Identifier: CA2036242213
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51921013G= , CM000674.2:g.51921013G= GRCh38
NC_000012.11:g.52314797G= , CM000674.1:g.52314797G= GRCh37
NC_000012.10:g.50601064G= NCBI36
NG_009549.1:g.18596G= , LRG_543:g.18596G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000551576.6:c.*120G= ENSP00000455848.2:n.*120G=
ENST00000388922.9:c.*120G= MANE Select ENSP00000373574.4:n.*120G=
ENST00000388922.8:c.*120G= ENSP00000373574.4:n.*120G=
ENST00000419526.6:c.*120G= ENSP00000392492.2:n.*120G=
ENST00000550683.5:c.*120G= ENSP00000447884.1:n.*120G=
NM_000020.2:c.*120G= , LRG_543t1:c.*120G= NP_000011.2:n.*120G=
NM_001077401.1:c.*120G= NP_001070869.1:n.*120G=
XM_005269235.2:c.*120G= XP_005269292.1:n.*120G=
XM_011539008.1:c.*120G= XP_011537310.1:n.*120G=
XM_024449279.1:c.*120G= XP_024305047.1:n.*120G=
NM_000020.3:c.*120G= MANE Select NP_000011.2:n.*120G=
NM_001077401.2:c.*120G= NP_001070869.1:n.*120G=