Canonical Allele Identifier: CA2036269440

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915282C= , CM000674.2:g.51915282C=	GRCh38
NC_000012.11:g.52309066C= , CM000674.1:g.52309066C=	GRCh37
NC_000012.10:g.50595333C=	NCBI36
NG_009549.1:g.12865C= , LRG_543:g.12865C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.560C=	ENSP00000446724.2:p.Thr187=
ENST00000551576.6:c.830C=	ENSP00000455848.2:p.Thr277=
ENST00000552678.2:c.830C=	ENSP00000457394.2:p.Thr277=
ENST00000388922.9:c.830C= MANE Select	ENSP00000373574.4:p.Thr277=
ENST00000388922.8:c.830C=	ENSP00000373574.4:p.Thr277=
ENST00000419526.6:c.308C=	ENSP00000392492.2:p.Thr103=
ENST00000550683.5:c.872C=	ENSP00000447884.1:p.Thr291=
NM_000020.2:c.830C= , LRG_543t1:c.830C=	NP_000011.2:p.Thr277=
NM_001077401.1:c.830C=	NP_001070869.1:p.Thr277=
XM_005269235.2:c.830C=	XP_005269292.1:p.Thr277=
XM_011539008.1:c.560C=	XP_011537310.1:p.Thr187=
XM_024449279.1:c.41C=	XP_024305047.1:p.Thr14=
NM_000020.3:c.830C= MANE Select	NP_000011.2:p.Thr277=
NM_001077401.2:c.830C=	NP_001070869.1:p.Thr277=