Canonical Allele Identifier: CA2036267431
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913357C= , CM000674.2:g.51913357C= GRCh38
NC_000012.11:g.52307141C= , CM000674.1:g.52307141C= GRCh37
NC_000012.10:g.50593408C= NCBI36
NG_009549.1:g.10940C= , LRG_543:g.10940C=

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.355+7C= ENSP00000446724.2:n.355+7C=
ENST00000551576.6:c.313+7C= ENSP00000455848.2:n.313+7C=
ENST00000552678.2:c.313+7C= ENSP00000457394.2:n.313+7C=
ENST00000388922.9:c.313+7C= MANE Select ENSP00000373574.4:n.313+7C=
ENST00000388922.8:c.313+7C= ENSP00000373574.4:n.313+7C=
ENST00000419526.6:c.103+822C= ENSP00000392492.2:n.103+822C=
ENST00000547400.5:c.355+7C= ENSP00000446724.1:n.355+7C=
ENST00000550683.5:c.355+7C= ENSP00000447884.1:n.355+7C=
NM_000020.2:c.313+7C= , LRG_543t1:c.313+7C= NP_000011.2:n.313+7C=
NM_001077401.1:c.313+7C= NP_001070869.1:n.313+7C=
XM_005269235.2:c.313+7C= XP_005269292.1:n.313+7C=
XM_011539008.1:c.355+7C= XP_011537310.1:n.355+7C=
XM_024449279.1:c.-377+7C= XP_024305047.1:n.-377+7C=
NM_000020.3:c.313+7C= MANE Select NP_000011.2:n.313+7C=
NM_001077401.2:c.313+7C= NP_001070869.1:n.313+7C=