Canonical Allele Identifier: CA2036242292
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51921119C= , CM000674.2:g.51921119C= GRCh38
NC_000012.11:g.52314903C= , CM000674.1:g.52314903C= GRCh37
NC_000012.10:g.50601170C= NCBI36
NG_009549.1:g.18702C= , LRG_543:g.18702C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000551576.6:c.*226C= ENSP00000455848.2:n.*226C=
ENST00000388922.9:c.*226C= MANE Select ENSP00000373574.4:n.*226C=
ENST00000419526.6:c.*226C= ENSP00000392492.2:n.*226C=
ENST00000550683.5:c.*226C= ENSP00000447884.1:n.*226C=
NM_000020.2:c.*226C= , LRG_543t1:c.*226C= NP_000011.2:n.*226C=
NM_001077401.1:c.*226C= NP_001070869.1:n.*226C=
XM_005269235.2:c.*226C= XP_005269292.1:n.*226C=
XM_011539008.1:c.*226C= XP_011537310.1:n.*226C=
XM_024449279.1:c.*226C= XP_024305047.1:n.*226C=
NM_000020.3:c.*226C= MANE Select NP_000011.2:n.*226C=
NM_001077401.2:c.*226C= NP_001070869.1:n.*226C=