Canonical Allele Identifier: CA2036268668
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51914248G= , CM000674.2:g.51914248G= GRCh38
NC_000012.11:g.52308032G= , CM000674.1:g.52308032G= GRCh37
NC_000012.10:g.50594299G= NCBI36
NG_009549.1:g.11831G= , LRG_543:g.11831G=

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.356-191G= ENSP00000446724.2:n.356-191G=
ENST00000551576.6:c.625+175G= ENSP00000455848.2:n.625+175G=
ENST00000552678.2:c.625+175G= ENSP00000457394.2:n.625+175G=
ENST00000388922.9:c.625+175G= MANE Select ENSP00000373574.4:n.625+175G=
ENST00000388922.8:c.625+175G= ENSP00000373574.4:n.625+175G=
ENST00000419526.6:c.104-191G= ENSP00000392492.2:n.104-191G=
ENST00000547400.5:c.356-191G= ENSP00000446724.1:n.356-191G=
ENST00000550683.5:c.667+175G= ENSP00000447884.1:n.667+175G=
NM_000020.2:c.625+175G= , LRG_543t1:c.625+175G= NP_000011.2:n.625+175G=
NM_001077401.1:c.625+175G= NP_001070869.1:n.625+175G=
XM_005269235.2:c.625+175G= XP_005269292.1:n.625+175G=
XM_011539008.1:c.356-191G= XP_011537310.1:n.356-191G=
XM_024449279.1:c.-164-191G= XP_024305047.1:n.-164-191G=
NM_000020.3:c.625+175G= MANE Select NP_000011.2:n.625+175G=
NM_001077401.2:c.625+175G= NP_001070869.1:n.625+175G=