Canonical Allele Identifier: CA2618857317
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51915208A>T , CM000674.2:g.51915208A>T GRCh38
NC_000012.11:g.52308992A>T , CM000674.1:g.52308992A>T GRCh37
NC_000012.10:g.50595259A>T NCBI36
NG_009549.1:g.12791A>T , LRG_543:g.12791A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.503-17A>T ENSP00000446724.2:n.503-17A>T
ENST00000551576.6:c.773-17A>T ENSP00000455848.2:n.773-17A>T
ENST00000552678.2:c.773-17A>T ENSP00000457394.2:n.773-17A>T
ENST00000388922.9:c.773-17A>T MANE Select ENSP00000373574.4:n.773-17A>T
ENST00000388922.8:c.773-17A>T ENSP00000373574.4:n.773-17A>T
ENST00000419526.6:c.251-17A>T ENSP00000392492.2:n.251-17A>T
ENST00000550683.5:c.815-17A>T ENSP00000447884.1:n.815-17A>T
NM_000020.2:c.773-17A>T , LRG_543t1:c.773-17A>T NP_000011.2:n.773-17A>T
NM_001077401.1:c.773-17A>T NP_001070869.1:n.773-17A>T
XM_005269235.2:c.773-17A>T XP_005269292.1:n.773-17A>T
XM_011539008.1:c.503-17A>T XP_011537310.1:n.503-17A>T
XM_024449279.1:c.-17-17A>T XP_024305047.1:n.-17-17A>T
NM_000020.3:c.773-17A>T MANE Select NP_000011.2:n.773-17A>T
NM_001077401.2:c.773-17A>T NP_001070869.1:n.773-17A>T