Canonical Allele Identifier: CA384902031
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51916048T>C , CM000674.2:g.51916048T>C GRCh38
NC_000012.11:g.52309832T>C , CM000674.1:g.52309832T>C GRCh37
NC_000012.10:g.50596099T>C NCBI36
NG_009549.1:g.13631T>C , LRG_543:g.13631T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.791T>C ENSP00000446724.2:p.Met264Thr
ENST00000551576.6:c.1061T>C ENSP00000455848.2:p.Met354Thr
ENST00000552678.2:c.1061T>C ENSP00000457394.2:p.Met354Thr
ENST00000388922.9:c.1061T>C MANE Select ENSP00000373574.4:p.Met354Thr
ENST00000388922.8:c.1061T>C ENSP00000373574.4:p.Met354Thr
ENST00000419526.6:c.539T>C ENSP00000392492.2:p.Met180Thr
ENST00000547632.1:n.336T>C
ENST00000550683.5:c.1103T>C ENSP00000447884.1:p.Met368Thr
ENST00000552678.1:c.66T>C
NM_000020.2:c.1061T>C , LRG_543t1:c.1061T>C NP_000011.2:p.Met354Thr
NM_001077401.1:c.1061T>C NP_001070869.1:p.Met354Thr
XM_005269235.2:c.1061T>C XP_005269292.1:p.Met354Thr
XM_011539008.1:c.791T>C XP_011537310.1:p.Met264Thr
XM_024449279.1:c.272T>C XP_024305047.1:p.Met91Thr
NM_000020.3:c.1061T>C MANE Select NP_000011.2:p.Met354Thr
NM_001077401.2:c.1061T>C NP_001070869.1:p.Met354Thr