Canonical Allele Identifier: CA2618859894

Gene: ACVRL1

Linked Data

• gnomAD v4: 12-51919149-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51919149G>C , CM000674.2:g.51919149G>C	GRCh38
NC_000012.11:g.52312933G>C , CM000674.1:g.52312933G>C	GRCh37
NC_000012.10:g.50599200G>C	NCBI36
NG_009549.1:g.16732G>C , LRG_543:g.16732G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.1107+34G>C	ENSP00000446724.2:n.1107+34G>C
ENST00000551576.6:c.1377+34G>C	ENSP00000455848.2:n.1377+34G>C
ENST00000552678.2:c.1411G>C	ENSP00000457394.2:p.Val471Leu
ENST00000388922.9:c.1377+34G>C MANE Select	ENSP00000373574.4:n.1377+34G>C
ENST00000388922.8:c.1377+34G>C	ENSP00000373574.4:n.1377+34G>C
ENST00000419526.6:c.855+34G>C	ENSP00000392492.2:n.855+34G>C
ENST00000547632.1:n.686G>C
ENST00000550683.5:c.1419+34G>C	ENSP00000447884.1:n.1419+34G>C
ENST00000552678.1:c.416G>C
NM_000020.2:c.1377+34G>C , LRG_543t1:c.1377+34G>C	NP_000011.2:n.1377+34G>C
NM_001077401.1:c.1377+34G>C	NP_001070869.1:n.1377+34G>C
XM_005269235.2:c.1377+34G>C	XP_005269292.1:n.1377+34G>C
XM_011539008.1:c.1107+34G>C	XP_011537310.1:n.1107+34G>C
XM_024449279.1:c.588+34G>C	XP_024305047.1:n.588+34G>C
NM_000020.3:c.1377+34G>C MANE Select	NP_000011.2:n.1377+34G>C
NM_001077401.2:c.1377+34G>C	NP_001070869.1:n.1377+34G>C