Canonical Allele Identifier: CA384899180
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913740A>T , CM000674.2:g.51913740A>T GRCh38
NC_000012.11:g.52307524A>T , CM000674.1:g.52307524A>T GRCh37
NC_000012.10:g.50593791A>T NCBI36
NG_009549.1:g.11323A>T , LRG_543:g.11323A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.355+390A>T ENSP00000446724.2:n.355+390A>T
ENST00000551576.6:c.495A>T ENSP00000455848.2:p.Lys165Asn
ENST00000552678.2:c.495A>T ENSP00000457394.2:p.Lys165Asn
ENST00000388922.9:c.495A>T MANE Select ENSP00000373574.4:p.Lys165Asn
ENST00000388922.8:c.495A>T ENSP00000373574.4:p.Lys165Asn
ENST00000419526.6:c.104-699A>T ENSP00000392492.2:n.104-699A>T
ENST00000547400.5:c.355+390A>T ENSP00000446724.1:n.355+390A>T
ENST00000550683.5:c.537A>T ENSP00000447884.1:p.Lys179Asn
NM_000020.2:c.495A>T , LRG_543t1:c.495A>T NP_000011.2:p.Lys165Asn
NM_001077401.1:c.495A>T NP_001070869.1:p.Lys165Asn
XM_005269235.2:c.495A>T XP_005269292.1:p.Lys165Asn
XM_011539008.1:c.355+390A>T XP_011537310.1:n.355+390A>T
XM_024449279.1:c.-195A>T XP_024305047.1:n.-195A>T
NM_000020.3:c.495A>T MANE Select NP_000011.2:p.Lys165Asn
NM_001077401.2:c.495A>T NP_001070869.1:p.Lys165Asn