Canonical Allele Identifier: CA2036269466
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51915332C= , CM000674.2:g.51915332C= GRCh38
NC_000012.11:g.52309116C= , CM000674.1:g.52309116C= GRCh37
NC_000012.10:g.50595383C= NCBI36
NG_009549.1:g.12915C= , LRG_543:g.12915C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.610C= ENSP00000446724.2:p.Leu204=
ENST00000551576.6:c.880C= ENSP00000455848.2:p.Leu294=
ENST00000552678.2:c.880C= ENSP00000457394.2:p.Leu294=
ENST00000388922.9:c.880C= MANE Select ENSP00000373574.4:p.Leu294=
ENST00000388922.8:c.880C= ENSP00000373574.4:p.Leu294=
ENST00000419526.6:c.358C= ENSP00000392492.2:p.Leu120=
ENST00000550683.5:c.922C= ENSP00000447884.1:p.Leu308=
NM_000020.2:c.880C= , LRG_543t1:c.880C= NP_000011.2:p.Leu294=
NM_001077401.1:c.880C= NP_001070869.1:p.Leu294=
XM_005269235.2:c.880C= XP_005269292.1:p.Leu294=
XM_011539008.1:c.610C= XP_011537310.1:p.Leu204=
XM_024449279.1:c.91C= XP_024305047.1:p.Leu31=
NM_000020.3:c.880C= MANE Select NP_000011.2:p.Leu294=
NM_001077401.2:c.880C= NP_001070869.1:p.Leu294=