Canonical Allele Identifier: CA479807879

Gene: ACVRL1

Linked Data

• gnomAD v4: 12-51914503-C-T
• MyVariant Identifiers: chr12:g.52308287C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51914503C>T , CM000674.2:g.51914503C>T	GRCh38
NC_000012.11:g.52308287C>T , CM000674.1:g.52308287C>T	GRCh37
NC_000012.10:g.50594554C>T	NCBI36
NG_009549.1:g.12086C>T , LRG_543:g.12086C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.420C>T	ENSP00000446724.2:p.Ile140=
ENST00000551576.6:c.690C>T	ENSP00000455848.2:p.Ile230=
ENST00000552678.2:c.690C>T	ENSP00000457394.2:p.Ile230=
ENST00000388922.9:c.690C>T MANE Select	ENSP00000373574.4:p.Ile230=
ENST00000388922.8:c.690C>T	ENSP00000373574.4:p.Ile230=
ENST00000419526.6:c.168C>T	ENSP00000392492.2:p.Ile56=
ENST00000547400.5:c.420C>T	ENSP00000446724.1:p.Ile140=
ENST00000550683.5:c.732C>T	ENSP00000447884.1:p.Ile244=
NM_000020.2:c.690C>T , LRG_543t1:c.690C>T	NP_000011.2:p.Ile230=
NM_001077401.1:c.690C>T	NP_001070869.1:p.Ile230=
XM_005269235.2:c.690C>T	XP_005269292.1:p.Ile230=
XM_011539008.1:c.420C>T	XP_011537310.1:p.Ile140=
XM_024449279.1:c.-100C>T	XP_024305047.1:n.-100C>T
NM_000020.3:c.690C>T MANE Select	NP_000011.2:p.Ile230=
NM_001077401.2:c.690C>T	NP_001070869.1:p.Ile230=