Canonical Allele Identifier: CA384901333
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51915416G>A , CM000674.2:g.51915416G>A GRCh38
NC_000012.11:g.52309200G>A , CM000674.1:g.52309200G>A GRCh37
NC_000012.10:g.50595467G>A NCBI36
NG_009549.1:g.12999G>A , LRG_543:g.12999G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.694G>A ENSP00000446724.2:p.Gly232Ser
ENST00000551576.6:c.964G>A ENSP00000455848.2:p.Gly322Ser
ENST00000552678.2:c.964G>A ENSP00000457394.2:p.Gly322Ser
ENST00000388922.9:c.964G>A MANE Select ENSP00000373574.4:p.Gly322Ser
ENST00000388922.8:c.964G>A ENSP00000373574.4:p.Gly322Ser
ENST00000419526.6:c.442G>A ENSP00000392492.2:p.Gly148Ser
ENST00000550683.5:c.1006G>A ENSP00000447884.1:p.Gly336Ser
NM_000020.2:c.964G>A , LRG_543t1:c.964G>A NP_000011.2:p.Gly322Ser
NM_001077401.1:c.964G>A NP_001070869.1:p.Gly322Ser
XM_005269235.2:c.964G>A XP_005269292.1:p.Gly322Ser
XM_011539008.1:c.694G>A XP_011537310.1:p.Gly232Ser
XM_024449279.1:c.175G>A XP_024305047.1:p.Gly59Ser
NM_000020.3:c.964G>A MANE Select NP_000011.2:p.Gly322Ser
NM_001077401.2:c.964G>A NP_001070869.1:p.Gly322Ser