Canonical Allele Identifier: CA384900707
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51915335G>T , CM000674.2:g.51915335G>T GRCh38
NC_000012.11:g.52309119G>T , CM000674.1:g.52309119G>T GRCh37
NC_000012.10:g.50595386G>T NCBI36
NG_009549.1:g.12918G>T , LRG_543:g.12918G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.613G>T ENSP00000446724.2:p.Glu205Ter
ENST00000551576.6:c.883G>T ENSP00000455848.2:p.Glu295Ter
ENST00000552678.2:c.883G>T ENSP00000457394.2:p.Glu295Ter
ENST00000388922.9:c.883G>T MANE Select ENSP00000373574.4:p.Glu295Ter
ENST00000388922.8:c.883G>T ENSP00000373574.4:p.Glu295Ter
ENST00000419526.6:c.361G>T ENSP00000392492.2:p.Glu121Ter
ENST00000550683.5:c.925G>T ENSP00000447884.1:p.Glu309Ter
NM_000020.2:c.883G>T , LRG_543t1:c.883G>T NP_000011.2:p.Glu295Ter
NM_001077401.1:c.883G>T NP_001070869.1:p.Glu295Ter
XM_005269235.2:c.883G>T XP_005269292.1:p.Glu295Ter
XM_011539008.1:c.613G>T XP_011537310.1:p.Glu205Ter
XM_024449279.1:c.94G>T XP_024305047.1:p.Glu32Ter
NM_000020.3:c.883G>T MANE Select NP_000011.2:p.Glu295Ter
NM_001077401.2:c.883G>T NP_001070869.1:p.Glu295Ter