Canonical Allele Identifier: CA2977854955
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913341dup , CM000674.2:g.51913341dup GRCh38
NC_000012.11:g.52307125dup , CM000674.1:g.52307125dup GRCh37
NC_000012.10:g.50593392dup NCBI36
NG_009549.1:g.10924dup , LRG_543:g.10924dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.346dup ENSP00000446724.2:p.Val116GlyfsTer19
ENST00000551576.6:c.304dup ENSP00000455848.2:p.Val102GlyfsTer?
ENST00000552678.2:c.304dup ENSP00000457394.2:p.Val102GlyfsTer?
ENST00000388922.9:c.304dup MANE Select ENSP00000373574.4:p.Val102GlyfsTer?
ENST00000388922.8:c.304dup ENSP00000373574.4:p.Val102GlyfsTer?
ENST00000419526.6:c.103+806dup ENSP00000392492.2:n.103+806dup
ENST00000547400.5:c.346dup ENSP00000446724.1:p.Val116GlyfsTer19
ENST00000550683.5:c.346dup ENSP00000447884.1:p.Val116GlyfsTer?
NM_000020.2:c.304dup , LRG_543t1:c.304dup NP_000011.2:p.Val102GlyfsTer?
NM_001077401.1:c.304dup NP_001070869.1:p.Val102GlyfsTer?
XM_005269235.2:c.304dup XP_005269292.1:p.Val102GlyfsTer?
XM_011539008.1:c.346dup XP_011537310.1:p.Val116GlyfsTer19
XM_024449279.1:c.-386dup XP_024305047.1:n.-386dup
NM_000020.3:c.304dup MANE Select NP_000011.2:p.Val102GlyfsTer?
NM_001077401.2:c.304dup NP_001070869.1:p.Val102GlyfsTer?