Canonical Allele Identifier: CA384900386
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51915255A>C , CM000674.2:g.51915255A>C GRCh38
NC_000012.11:g.52309039A>C , CM000674.1:g.52309039A>C GRCh37
NC_000012.10:g.50595306A>C NCBI36
NG_009549.1:g.12838A>C , LRG_543:g.12838A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.533A>C ENSP00000446724.2:p.Asn178Thr
ENST00000551576.6:c.803A>C ENSP00000455848.2:p.Asn268Thr
ENST00000552678.2:c.803A>C ENSP00000457394.2:p.Asn268Thr
ENST00000388922.9:c.803A>C MANE Select ENSP00000373574.4:p.Asn268Thr
ENST00000388922.8:c.803A>C ENSP00000373574.4:p.Asn268Thr
ENST00000419526.6:c.281A>C ENSP00000392492.2:p.Asn94Thr
ENST00000550683.5:c.845A>C ENSP00000447884.1:p.Asn282Thr
NM_000020.2:c.803A>C , LRG_543t1:c.803A>C NP_000011.2:p.Asn268Thr
NM_001077401.1:c.803A>C NP_001070869.1:p.Asn268Thr
XM_005269235.2:c.803A>C XP_005269292.1:p.Asn268Thr
XM_011539008.1:c.533A>C XP_011537310.1:p.Asn178Thr
XM_024449279.1:c.14A>C XP_024305047.1:p.Asn5Thr
NM_000020.3:c.803A>C MANE Select NP_000011.2:p.Asn268Thr
NM_001077401.2:c.803A>C NP_001070869.1:p.Asn268Thr