Canonical Allele Identifier: CA2618860736
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51920937_51920938insTGGGGGGGG , CM000674.2:g.51920937_51920938insTGGGGGGGG GRCh38
NC_000012.11:g.52314721_52314722insTGGGGGGGG , CM000674.1:g.52314721_52314722insTGGGGGGGG GRCh37
NC_000012.10:g.50600988_50600989insTGGGGGGGG NCBI36
NG_009549.1:g.18520_18521insTGGGGGGGG , LRG_543:g.18520_18521insTGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000551576.6:c.*44_*45insTGGGGGGGG ENSP00000455848.2:n.*44_*45insTGGGGGGGG
ENST00000388922.9:c.*44_*45insTGGGGGGGG MANE Select ENSP00000373574.4:n.*44_*45insTGGGGGGGG
ENST00000388922.8:c.*44_*45insTGGGGGGGG ENSP00000373574.4:n.*44_*45insTGGGGGGGG
ENST00000419526.6:c.*44_*45insTGGGGGGGG ENSP00000392492.2:n.*44_*45insTGGGGGGGG
ENST00000550683.5:c.*44_*45insTGGGGGGGG ENSP00000447884.1:n.*44_*45insTGGGGGGGG
NM_000020.2:c.*44_*45insTGGGGGGGG , LRG_543t1:c.*44_*45insTGGGGGGGG NP_000011.2:n.*44_*45insTGGGGGGGG
NM_001077401.1:c.*44_*45insTGGGGGGGG NP_001070869.1:n.*44_*45insTGGGGGGGG
XM_005269235.2:c.*44_*45insTGGGGGGGG XP_005269292.1:n.*44_*45insTGGGGGGGG
XM_011539008.1:c.*44_*45insTGGGGGGGG XP_011537310.1:n.*44_*45insTGGGGGGGG
XM_024449279.1:c.*44_*45insTGGGGGGGG XP_024305047.1:n.*44_*45insTGGGGGGGG
NM_000020.3:c.*44_*45insTGGGGGGGG MANE Select NP_000011.2:n.*44_*45insTGGGGGGGG
NM_001077401.2:c.*44_*45insTGGGGGGGG NP_001070869.1:n.*44_*45insTGGGGGGGG