Canonical Allele Identifier: CA384898084

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913323A>G , CM000674.2:g.51913323A>G	GRCh38
NC_000012.11:g.52307107A>G , CM000674.1:g.52307107A>G	GRCh37
NC_000012.10:g.50593374A>G	NCBI36
NG_009549.1:g.10906A>G , LRG_543:g.10906A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.328A>G	ENSP00000446724.2:p.Asn110Asp
ENST00000551576.6:c.286A>G	ENSP00000455848.2:p.Asn96Asp
ENST00000552678.2:c.286A>G	ENSP00000457394.2:p.Asn96Asp
ENST00000388922.9:c.286A>G MANE Select	ENSP00000373574.4:p.Asn96Asp
ENST00000388922.8:c.286A>G	ENSP00000373574.4:p.Asn96Asp
ENST00000419526.6:c.103+788A>G	ENSP00000392492.2:n.103+788A>G
ENST00000547400.5:c.328A>G	ENSP00000446724.1:p.Asn110Asp
ENST00000550683.5:c.328A>G	ENSP00000447884.1:p.Asn110Asp
NM_000020.2:c.286A>G , LRG_543t1:c.286A>G	NP_000011.2:p.Asn96Asp
NM_001077401.1:c.286A>G	NP_001070869.1:p.Asn96Asp
XM_005269235.2:c.286A>G	XP_005269292.1:p.Asn96Asp
XM_011539008.1:c.328A>G	XP_011537310.1:p.Asn110Asp
XM_024449279.1:c.-404A>G	XP_024305047.1:n.-404A>G
NM_000020.3:c.286A>G MANE Select	NP_000011.2:p.Asn96Asp
NM_001077401.2:c.286A>G	NP_001070869.1:p.Asn96Asp