Canonical Allele Identifier: CA6573025

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 1767454
• ClinVar RCV Id: RCV002385236
• dbSNP Id: rs778954562
• ExAC: 12:52309193 T / C
• gnomAD v2: 12-52309193-T-C
• gnomAD v3: 12-51915409-T-C
• gnomAD v4: 12-51915409-T-C
• MyVariant Identifiers: chr12:g.52309193T>C (hg19) ; chr12:g.51915409T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915409T>C , CM000674.2:g.51915409T>C	GRCh38
NC_000012.11:g.52309193T>C , CM000674.1:g.52309193T>C	GRCh37
NC_000012.10:g.50595460T>C	NCBI36
NG_009549.1:g.12992T>C , LRG_543:g.12992T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.687T>C	ENSP00000446724.2:p.Gly229=
ENST00000551576.6:c.957T>C	ENSP00000455848.2:p.Gly319=
ENST00000552678.2:c.957T>C	ENSP00000457394.2:p.Gly319=
ENST00000388922.9:c.957T>C MANE Select	ENSP00000373574.4:p.Gly319=
ENST00000388922.8:c.957T>C	ENSP00000373574.4:p.Gly319=
ENST00000419526.6:c.435T>C	ENSP00000392492.2:p.Gly145=
ENST00000550683.5:c.999T>C	ENSP00000447884.1:p.Gly333=
NM_000020.2:c.957T>C , LRG_543t1:c.957T>C	NP_000011.2:p.Gly319=
NM_001077401.1:c.957T>C	NP_001070869.1:p.Gly319=
XM_005269235.2:c.957T>C	XP_005269292.1:p.Gly319=
XM_011539008.1:c.687T>C	XP_011537310.1:p.Gly229=
XM_024449279.1:c.168T>C	XP_024305047.1:p.Gly56=
NM_000020.3:c.957T>C MANE Select	NP_000011.2:p.Gly319=
NM_001077401.2:c.957T>C	NP_001070869.1:p.Gly319=