Canonical Allele Identifier: CA2036239784
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51919030A= , CM000674.2:g.51919030A= GRCh38
NC_000012.11:g.52312814A= , CM000674.1:g.52312814A= GRCh37
NC_000012.10:g.50599081A= NCBI36
NG_009549.1:g.16613A= , LRG_543:g.16613A=

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.1022A= ENSP00000446724.2:p.Asn341=
ENST00000551576.6:c.1292A= ENSP00000455848.2:p.Asn431=
ENST00000552678.2:c.1292A= ENSP00000457394.2:p.Asn431=
ENST00000388922.9:c.1292A= MANE Select ENSP00000373574.4:p.Asn431=
ENST00000388922.8:c.1292A= ENSP00000373574.4:p.Asn431=
ENST00000419526.6:c.770A= ENSP00000392492.2:p.Asn257=
ENST00000547632.1:n.567A=
ENST00000550683.5:c.1334A= ENSP00000447884.1:p.Asn445=
ENST00000552678.1:c.297A=
NM_000020.2:c.1292A= , LRG_543t1:c.1292A= NP_000011.2:p.Asn431=
NM_001077401.1:c.1292A= NP_001070869.1:p.Asn431=
XM_005269235.2:c.1292A= XP_005269292.1:p.Asn431=
XM_011539008.1:c.1022A= XP_011537310.1:p.Asn341=
XM_024449279.1:c.503A= XP_024305047.1:p.Asn168=
NM_000020.3:c.1292A= MANE Select NP_000011.2:p.Asn431=
NM_001077401.2:c.1292A= NP_001070869.1:p.Asn431=