Canonical Allele Identifier: CA2036267462
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913372C= , CM000674.2:g.51913372C= GRCh38
NC_000012.11:g.52307156C= , CM000674.1:g.52307156C= GRCh37
NC_000012.10:g.50593423C= NCBI36
NG_009549.1:g.10955C= , LRG_543:g.10955C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.355+22C= ENSP00000446724.2:n.355+22C=
ENST00000551576.6:c.313+22C= ENSP00000455848.2:n.313+22C=
ENST00000552678.2:c.313+22C= ENSP00000457394.2:n.313+22C=
ENST00000388922.9:c.313+22C= MANE Select ENSP00000373574.4:n.313+22C=
ENST00000388922.8:c.313+22C= ENSP00000373574.4:n.313+22C=
ENST00000419526.6:c.103+837C= ENSP00000392492.2:n.103+837C=
ENST00000547400.5:c.355+22C= ENSP00000446724.1:n.355+22C=
ENST00000550683.5:c.355+22C= ENSP00000447884.1:n.355+22C=
NM_000020.2:c.313+22C= , LRG_543t1:c.313+22C= NP_000011.2:n.313+22C=
NM_001077401.1:c.313+22C= NP_001070869.1:n.313+22C=
XM_005269235.2:c.313+22C= XP_005269292.1:n.313+22C=
XM_011539008.1:c.355+22C= XP_011537310.1:n.355+22C=
XM_024449279.1:c.-377+22C= XP_024305047.1:n.-377+22C=
NM_000020.3:c.313+22C= MANE Select NP_000011.2:n.313+22C=
NM_001077401.2:c.313+22C= NP_001070869.1:n.313+22C=