Canonical Allele Identifier: CA2036268258
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913984A= , CM000674.2:g.51913984A= GRCh38
NC_000012.11:g.52307768A= , CM000674.1:g.52307768A= GRCh37
NC_000012.10:g.50594035A= NCBI36
NG_009549.1:g.11567A= , LRG_543:g.11567A=

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.356-455A= ENSP00000446724.2:n.356-455A=
ENST00000551576.6:c.536A= ENSP00000455848.2:p.Asp179=
ENST00000552678.2:c.536A= ENSP00000457394.2:p.Asp179=
ENST00000388922.9:c.536A= MANE Select ENSP00000373574.4:p.Asp179=
ENST00000388922.8:c.536A= ENSP00000373574.4:p.Asp179=
ENST00000419526.6:c.104-455A= ENSP00000392492.2:n.104-455A=
ENST00000547400.5:c.356-455A= ENSP00000446724.1:n.356-455A=
ENST00000550683.5:c.578A= ENSP00000447884.1:p.Asp193=
NM_000020.2:c.536A= , LRG_543t1:c.536A= NP_000011.2:p.Asp179=
NM_001077401.1:c.536A= NP_001070869.1:p.Asp179=
XM_005269235.2:c.536A= XP_005269292.1:p.Asp179=
XM_011539008.1:c.356-455A= XP_011537310.1:n.356-455A=
XM_024449279.1:c.-165+214A= XP_024305047.1:n.-165+214A=
NM_000020.3:c.536A= MANE Select NP_000011.2:p.Asp179=
NM_001077401.2:c.536A= NP_001070869.1:p.Asp179=