Canonical Allele Identifier: CA2795983830

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51920925_51920926insTGGGGGGGGGGGGG , CM000674.2:g.51920925_51920926insTGGGGGGGGGGGGG	GRCh38
NC_000012.11:g.52314709_52314710insTGGGGGGGGGGGGG , CM000674.1:g.52314709_52314710insTGGGGGGGGGGGGG	GRCh37
NC_000012.10:g.50600976_50600977insTGGGGGGGGGGGGG	NCBI36
NG_009549.1:g.18508_18509insTGGGGGGGGGGGGG , LRG_543:g.18508_18509insTGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551576.6:c.*32_*33insTGGGGGGGGGGGGG	ENSP00000455848.2:n.*32_*33insTGGGGGGGGGGGGG
ENST00000388922.9:c.*32_*33insTGGGGGGGGGGGGG MANE Select	ENSP00000373574.4:n.*32_*33insTGGGGGGGGGGGGG
ENST00000388922.8:c.*32_*33insTGGGGGGGGGGGGG	ENSP00000373574.4:n.*32_*33insTGGGGGGGGGGGGG
ENST00000419526.6:c.*32_*33insTGGGGGGGGGGGGG	ENSP00000392492.2:n.*32_*33insTGGGGGGGGGGGGG
ENST00000550683.5:c.*32_*33insTGGGGGGGGGGGGG	ENSP00000447884.1:n.*32_*33insTGGGGGGGGGGGGG
NM_000020.2:c.*32_*33insTGGGGGGGGGGGGG , LRG_543t1:c.*32_*33insTGGGGGGGGGGGGG	NP_000011.2:n.*32_*33insTGGGGGGGGGGGGG
NM_001077401.1:c.*32_*33insTGGGGGGGGGGGGG	NP_001070869.1:n.*32_*33insTGGGGGGGGGGGGG
XM_005269235.2:c.*32_*33insTGGGGGGGGGGGGG	XP_005269292.1:n.*32_*33insTGGGGGGGGGGGGG
XM_011539008.1:c.*32_*33insTGGGGGGGGGGGGG	XP_011537310.1:n.*32_*33insTGGGGGGGGGGGGG
XM_024449279.1:c.*32_*33insTGGGGGGGGGGGGG	XP_024305047.1:n.*32_*33insTGGGGGGGGGGGGG
NM_000020.3:c.*32_*33insTGGGGGGGGGGGGG MANE Select	NP_000011.2:n.*32_*33insTGGGGGGGGGGGGG
NM_001077401.2:c.*32_*33insTGGGGGGGGGGGGG	NP_001070869.1:n.*32_*33insTGGGGGGGGGGGGG