Canonical Allele Identifier: CA3192155745

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913339T= , CM000674.2:g.51913339T=	GRCh38
NC_000012.11:g.52307123T= , CM000674.1:g.52307123T=	GRCh37
NC_000012.10:g.50593390T=	NCBI36
NG_009549.1:g.10922T= , LRG_543:g.10922T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000020.3:c.302T= MANE Select	NP_000011.2:p.Leu101=
ENST00000388922.9:c.302T= MANE Select	ENSP00000373574.4:p.Leu101=
NM_000020.2:c.302T= , LRG_543t1:c.302T=	NP_000011.2:p.Leu101=
NM_001077401.1:c.302T=	NP_001070869.1:p.Leu101=
NM_001077401.2:c.302T=	NP_001070869.1:p.Leu101=
ENST00000388922.8:c.302T=	ENSP00000373574.4:p.Leu101=
ENST00000419526.6:c.103+804T=	ENSP00000392492.2:n.103+804T=
ENST00000547400.5:c.344T=	ENSP00000446724.1:p.Leu115=
ENST00000547400.6:c.344T=	ENSP00000446724.2:p.Leu115=
ENST00000550683.5:c.344T=	ENSP00000447884.1:p.Leu115=
ENST00000551576.6:c.302T=	ENSP00000455848.2:p.Leu101=
ENST00000552678.2:c.302T=	ENSP00000457394.2:p.Leu101=
XM_005269235.2:c.302T=	XP_005269292.1:p.Leu101=
XM_011539008.1:c.344T=	XP_011537310.1:p.Leu115=
XM_024449279.1:c.-388T=	XP_024305047.1:n.-388T=