Canonical Allele Identifier: CA384906335

Gene: ACVRL1

Linked Data

• MyVariant Identifiers: chr12:g.52314670T>A (hg19) ; chr12:g.51920886T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51920886T>A , CM000674.2:g.51920886T>A	GRCh38
NC_000012.11:g.52314670T>A , CM000674.1:g.52314670T>A	GRCh37
NC_000012.10:g.50600937T>A	NCBI36
NG_009549.1:g.18469T>A , LRG_543:g.18469T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.1235T>A	ENSP00000446724.2:p.Ile412Asn
ENST00000551576.6:c.1505T>A	ENSP00000455848.2:p.Ile502Asn
ENST00000388922.9:c.1505T>A MANE Select	ENSP00000373574.4:p.Ile502Asn
ENST00000388922.8:c.1505T>A	ENSP00000373574.4:p.Ile502Asn
ENST00000419526.6:c.983T>A	ENSP00000392492.2:p.Ile328Asn
ENST00000550683.5:c.1547T>A	ENSP00000447884.1:p.Ile516Asn
NM_000020.2:c.1505T>A , LRG_543t1:c.1505T>A	NP_000011.2:p.Ile502Asn
NM_001077401.1:c.1505T>A	NP_001070869.1:p.Ile502Asn
XM_005269235.2:c.1505T>A	XP_005269292.1:p.Ile502Asn
XM_011539008.1:c.1235T>A	XP_011537310.1:p.Ile412Asn
XM_024449279.1:c.716T>A	XP_024305047.1:p.Ile239Asn
NM_000020.3:c.1505T>A MANE Select	NP_000011.2:p.Ile502Asn
NM_001077401.2:c.1505T>A	NP_001070869.1:p.Ile502Asn