Canonical Allele Identifier: CA2036269411
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51915212T= , CM000674.2:g.51915212T= GRCh38
NC_000012.11:g.52308996T= , CM000674.1:g.52308996T= GRCh37
NC_000012.10:g.50595263T= NCBI36
NG_009549.1:g.12795T= , LRG_543:g.12795T=

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.503-13T= ENSP00000446724.2:n.503-13T=
ENST00000551576.6:c.773-13T= ENSP00000455848.2:n.773-13T=
ENST00000552678.2:c.773-13T= ENSP00000457394.2:n.773-13T=
ENST00000388922.9:c.773-13T= MANE Select ENSP00000373574.4:n.773-13T=
ENST00000388922.8:c.773-13T= ENSP00000373574.4:n.773-13T=
ENST00000419526.6:c.251-13T= ENSP00000392492.2:n.251-13T=
ENST00000550683.5:c.815-13T= ENSP00000447884.1:n.815-13T=
NM_000020.2:c.773-13T= , LRG_543t1:c.773-13T= NP_000011.2:n.773-13T=
NM_001077401.1:c.773-13T= NP_001070869.1:n.773-13T=
XM_005269235.2:c.773-13T= XP_005269292.1:n.773-13T=
XM_011539008.1:c.503-13T= XP_011537310.1:n.503-13T=
XM_024449279.1:c.-17-13T= XP_024305047.1:n.-17-13T=
NM_000020.3:c.773-13T= MANE Select NP_000011.2:n.773-13T=
NM_001077401.2:c.773-13T= NP_001070869.1:n.773-13T=