Canonical Allele Identifier: CA2036267376
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913340G= , CM000674.2:g.51913340G= GRCh38
NC_000012.11:g.52307124G= , CM000674.1:g.52307124G= GRCh37
NC_000012.10:g.50593391G= NCBI36
NG_009549.1:g.10923G= , LRG_543:g.10923G=

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.345G= ENSP00000446724.2:p.Leu115=
ENST00000551576.6:c.303G= ENSP00000455848.2:p.Leu101=
ENST00000552678.2:c.303G= ENSP00000457394.2:p.Leu101=
ENST00000388922.9:c.303G= MANE Select ENSP00000373574.4:p.Leu101=
ENST00000388922.8:c.303G= ENSP00000373574.4:p.Leu101=
ENST00000419526.6:c.103+805G= ENSP00000392492.2:n.103+805G=
ENST00000547400.5:c.345G= ENSP00000446724.1:p.Leu115=
ENST00000550683.5:c.345G= ENSP00000447884.1:p.Leu115=
NM_000020.2:c.303G= , LRG_543t1:c.303G= NP_000011.2:p.Leu101=
NM_001077401.1:c.303G= NP_001070869.1:p.Leu101=
XM_005269235.2:c.303G= XP_005269292.1:p.Leu101=
XM_011539008.1:c.345G= XP_011537310.1:p.Leu115=
XM_024449279.1:c.-387G= XP_024305047.1:n.-387G=
NM_000020.3:c.303G= MANE Select NP_000011.2:p.Leu101=
NM_001077401.2:c.303G= NP_001070869.1:p.Leu101=