Canonical Allele Identifier: CA2795983138
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51915994_51916016del , CM000674.2:g.51915994_51916016del GRCh38
NC_000012.11:g.52309778_52309800del , CM000674.1:g.52309778_52309800del GRCh37
NC_000012.10:g.50596045_50596067del NCBI36
NG_009549.1:g.13577_13599del , LRG_543:g.13577_13599del

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.779-42_779-20del ENSP00000446724.2:n.779-42_779-20del
ENST00000551576.6:c.1049-42_1049-20del ENSP00000455848.2:n.1049-42_1049-20del
ENST00000552678.2:c.1049-42_1049-20del ENSP00000457394.2:n.1049-42_1049-20del
ENST00000388922.9:c.1049-42_1049-20del MANE Select ENSP00000373574.4:n.1049-42_1049-20del
ENST00000388922.8:c.1049-42_1049-20del ENSP00000373574.4:n.1049-42_1049-20del
ENST00000419526.6:c.527-42_527-20del ENSP00000392492.2:n.527-42_527-20del
ENST00000547632.1:n.282_304del
ENST00000550683.5:c.1091-42_1091-20del ENSP00000447884.1:n.1091-42_1091-20del
ENST00000552678.1:c.54-42_54-20del
NM_000020.2:c.1049-42_1049-20del , LRG_543t1:c.1049-42_1049-20del NP_000011.2:n.1049-42_1049-20del
NM_001077401.1:c.1049-42_1049-20del NP_001070869.1:n.1049-42_1049-20del
XM_005269235.2:c.1049-42_1049-20del XP_005269292.1:n.1049-42_1049-20del
XM_011539008.1:c.779-42_779-20del XP_011537310.1:n.779-42_779-20del
XM_024449279.1:c.260-42_260-20del XP_024305047.1:n.260-42_260-20del
NM_000020.3:c.1049-42_1049-20del MANE Select NP_000011.2:n.1049-42_1049-20del
NM_001077401.2:c.1049-42_1049-20del NP_001070869.1:n.1049-42_1049-20del