Canonical Allele Identifier: CA2036269468
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51915338C= , CM000674.2:g.51915338C= GRCh38
NC_000012.11:g.52309122C= , CM000674.1:g.52309122C= GRCh37
NC_000012.10:g.50595389C= NCBI36
NG_009549.1:g.12921C= , LRG_543:g.12921C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.616C= ENSP00000446724.2:p.Pro206=
ENST00000551576.6:c.886C= ENSP00000455848.2:p.Pro296=
ENST00000552678.2:c.886C= ENSP00000457394.2:p.Pro296=
ENST00000388922.9:c.886C= MANE Select ENSP00000373574.4:p.Pro296=
ENST00000388922.8:c.886C= ENSP00000373574.4:p.Pro296=
ENST00000419526.6:c.364C= ENSP00000392492.2:p.Pro122=
ENST00000550683.5:c.928C= ENSP00000447884.1:p.Pro310=
NM_000020.2:c.886C= , LRG_543t1:c.886C= NP_000011.2:p.Pro296=
NM_001077401.1:c.886C= NP_001070869.1:p.Pro296=
XM_005269235.2:c.886C= XP_005269292.1:p.Pro296=
XM_011539008.1:c.616C= XP_011537310.1:p.Pro206=
XM_024449279.1:c.97C= XP_024305047.1:p.Pro33=
NM_000020.3:c.886C= MANE Select NP_000011.2:p.Pro296=
NM_001077401.2:c.886C= NP_001070869.1:p.Pro296=