Canonical Allele Identifier: CA384900091
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51914507T>A , CM000674.2:g.51914507T>A GRCh38
NC_000012.11:g.52308291T>A , CM000674.1:g.52308291T>A GRCh37
NC_000012.10:g.50594558T>A NCBI36
NG_009549.1:g.12090T>A , LRG_543:g.12090T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000547400.6:c.424T>A ENSP00000446724.2:p.Ser142Thr
ENST00000551576.6:c.694T>A ENSP00000455848.2:p.Ser232Thr
ENST00000552678.2:c.694T>A ENSP00000457394.2:p.Ser232Thr
ENST00000388922.9:c.694T>A MANE Select ENSP00000373574.4:p.Ser232Thr
ENST00000388922.8:c.694T>A ENSP00000373574.4:p.Ser232Thr
ENST00000419526.6:c.172T>A ENSP00000392492.2:p.Ser58Thr
ENST00000547400.5:c.424T>A ENSP00000446724.1:p.Ser142Thr
ENST00000550683.5:c.736T>A ENSP00000447884.1:p.Ser246Thr
NM_000020.2:c.694T>A , LRG_543t1:c.694T>A NP_000011.2:p.Ser232Thr
NM_001077401.1:c.694T>A NP_001070869.1:p.Ser232Thr
XM_005269235.2:c.694T>A XP_005269292.1:p.Ser232Thr
XM_011539008.1:c.424T>A XP_011537310.1:p.Ser142Thr
XM_024449279.1:c.-96T>A XP_024305047.1:n.-96T>A
NM_000020.3:c.694T>A MANE Select NP_000011.2:p.Ser232Thr
NM_001077401.2:c.694T>A NP_001070869.1:p.Ser232Thr