Canonical Allele Identifier: CA2575161222
Gene: ACVRL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51912333G>T , CM000674.2:g.51912333G>T GRCh38
NC_000012.11:g.52306117G>T , CM000674.1:g.52306117G>T GRCh37
NC_000012.10:g.50592384G>T NCBI36
NG_009549.1:g.9916G>T , LRG_543:g.9916G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.-100G>T ENSP00000446724.2:n.-100G>T
ENST00000551576.6:c.-5-137G>T ENSP00000455848.2:n.-5-137G>T
ENST00000552678.2:c.-5-137G>T ENSP00000457394.2:n.-5-137G>T
ENST00000388922.9:c.-5-137G>T MANE Select ENSP00000373574.4:n.-5-137G>T
ENST00000388922.8:c.-5-137G>T ENSP00000373574.4:n.-5-137G>T
ENST00000547400.5:c.-100G>T ENSP00000446724.1:n.-100G>T
ENST00000550683.5:c.-100G>T ENSP00000447884.1:n.-100G>T
ENST00000551576.5:c.-5-137G>T ENSP00000455848.1:n.-5-137G>T
NM_000020.2:c.-5-137G>T , LRG_543t1:c.-5-137G>T NP_000011.2:n.-5-137G>T
NM_001077401.1:c.-142G>T NP_001070869.1:n.-142G>T
XM_005269235.2:c.-5-137G>T XP_005269292.1:n.-5-137G>T
NM_000020.3:c.-5-137G>T MANE Select NP_000011.2:n.-5-137G>T