Canonical Allele Identifier: CA2695216692
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913619_51913620dup , CM000674.2:g.51913619_51913620dup GRCh38
NC_000012.11:g.52307403_52307404dup , CM000674.1:g.52307403_52307404dup GRCh37
NC_000012.10:g.50593670_50593671dup NCBI36
NG_009549.1:g.11202_11203dup , LRG_543:g.11202_11203dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.355+269_355+270dup ENSP00000446724.2:n.355+269_355+270dup
ENST00000551576.6:c.374_375dup ENSP00000455848.2:p.Val126ProfsTer?
ENST00000552678.2:c.374_375dup ENSP00000457394.2:p.Val126ProfsTer?
ENST00000388922.9:c.374_375dup MANE Select ENSP00000373574.4:p.Val126ProfsTer?
ENST00000388922.8:c.374_375dup ENSP00000373574.4:p.Val126ProfsTer?
ENST00000419526.6:c.104-820_104-819dup ENSP00000392492.2:n.104-820_104-819dup
ENST00000547400.5:c.355+269_355+270dup ENSP00000446724.1:n.355+269_355+270dup
ENST00000550683.5:c.416_417dup ENSP00000447884.1:p.Val140ProfsTer?
NM_000020.2:c.374_375dup , LRG_543t1:c.374_375dup NP_000011.2:p.Val126ProfsTer?
NM_001077401.1:c.374_375dup NP_001070869.1:p.Val126ProfsTer?
XM_005269235.2:c.374_375dup XP_005269292.1:p.Val126ProfsTer?
XM_011539008.1:c.355+269_355+270dup XP_011537310.1:n.355+269_355+270dup
XM_024449279.1:c.-316_-315dup XP_024305047.1:n.-316_-315dup
NM_000020.3:c.374_375dup MANE Select NP_000011.2:p.Val126ProfsTer?
NM_001077401.2:c.374_375dup NP_001070869.1:p.Val126ProfsTer?