Canonical Allele Identifier: CA2036236855

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51916103C= , CM000674.2:g.51916103C=	GRCh38
NC_000012.11:g.52309887C= , CM000674.1:g.52309887C=	GRCh37
NC_000012.10:g.50596154C=	NCBI36
NG_009549.1:g.13686C= , LRG_543:g.13686C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.846C=	ENSP00000446724.2:p.Thr282=
ENST00000551576.6:c.1116C=	ENSP00000455848.2:p.Thr372=
ENST00000552678.2:c.1116C=	ENSP00000457394.2:p.Thr372=
ENST00000388922.9:c.1116C= MANE Select	ENSP00000373574.4:p.Thr372=
ENST00000388922.8:c.1116C=	ENSP00000373574.4:p.Thr372=
ENST00000419526.6:c.594C=	ENSP00000392492.2:p.Thr198=
ENST00000547632.1:n.391C=
ENST00000550683.5:c.1158C=	ENSP00000447884.1:p.Thr386=
ENST00000552678.1:c.121C=
NM_000020.2:c.1116C= , LRG_543t1:c.1116C=	NP_000011.2:p.Thr372=
NM_001077401.1:c.1116C=	NP_001070869.1:p.Thr372=
XM_005269235.2:c.1116C=	XP_005269292.1:p.Thr372=
XM_011539008.1:c.846C=	XP_011537310.1:p.Thr282=
XM_024449279.1:c.327C=	XP_024305047.1:p.Thr109=
NM_000020.3:c.1116C= MANE Select	NP_000011.2:p.Thr372=
NM_001077401.2:c.1116C=	NP_001070869.1:p.Thr372=