Canonical Allele Identifier: CA384905830
Gene: ACVRL1 HGNC NCBI

Linked Data

dbSNP Id: rs1197652795

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920834A>G , CM000674.2:g.51920834A>G GRCh38
NC_000012.11:g.52314618A>G , CM000674.1:g.52314618A>G GRCh37
NC_000012.10:g.50600885A>G NCBI36
NG_009549.1:g.18417A>G , LRG_543:g.18417A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.1183A>G ENSP00000446724.2:p.Ile395Val
ENST00000551576.6:c.1453A>G ENSP00000455848.2:p.Ile485Val
ENST00000388922.9:c.1453A>G MANE Select ENSP00000373574.4:p.Ile485Val
ENST00000388922.8:c.1453A>G ENSP00000373574.4:p.Ile485Val
ENST00000419526.6:c.931A>G ENSP00000392492.2:p.Ile311Val
ENST00000550683.5:c.1495A>G ENSP00000447884.1:p.Ile499Val
NM_000020.2:c.1453A>G , LRG_543t1:c.1453A>G NP_000011.2:p.Ile485Val
NM_001077401.1:c.1453A>G NP_001070869.1:p.Ile485Val
XM_005269235.2:c.1453A>G XP_005269292.1:p.Ile485Val
XM_011539008.1:c.1183A>G XP_011537310.1:p.Ile395Val
XM_024449279.1:c.664A>G XP_024305047.1:p.Ile222Val
NM_000020.3:c.1453A>G MANE Select NP_000011.2:p.Ile485Val
NM_001077401.2:c.1453A>G NP_001070869.1:p.Ile485Val