Canonical Allele Identifier: CA95732988

Gene: LIAS

Linked Data

• ClinVar Variation Id: 675220
• ClinVar RCV Id: RCV000834574
• dbSNP Id: rs141807941
• gnomAD v2: 4-39474655-A-G
• gnomAD v3: 4-39473035-A-G
• gnomAD v4: 4-39473035-A-G
• MyVariant Identifiers: chr4:g.39474655A>G (hg19) ; chr4:g.39473035A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39473035A>G , CM000666.2:g.39473035A>G	GRCh38
NC_000004.11:g.39474655A>G , CM000666.1:g.39474655A>G	GRCh37
NC_000004.10:g.39151050A>G	NCBI36
NG_032111.1:g.18991A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261434.8:c.646-65A>G	ENSP00000261434.4:n.646-65A>G
ENST00000340169.7:c.954+1729A>G	ENSP00000340676.2:n.954+1729A>G
ENST00000381846.2:c.826-65A>G	ENSP00000371270.1:n.826-65A>G
ENST00000513731.6:c.565-65A>G	ENSP00000425580.1:n.565-65A>G
ENST00000638422.1:c.*478-65A>G	ENSP00000491001.1:n.*478-65A>G
ENST00000638430.1:c.652-65A>G
ENST00000638451.1:c.517-65A>G	ENSP00000491681.1:n.517-65A>G
ENST00000638816.1:c.669-65A>G	ENSP00000492482.1:n.669-65A>G
ENST00000639422.1:c.*311-65A>G	ENSP00000491899.1:n.*311-65A>G
ENST00000639475.1:n.1008-65A>G
ENST00000639614.1:n.149-65A>G
ENST00000640349.1:c.841-65A>G	ENSP00000491477.1:n.841-65A>G
ENST00000640381.1:n.1796-65A>G
ENST00000640672.1:c.586-65A>G	ENSP00000492203.1:n.586-65A>G
ENST00000640689.1:c.*1338+1729A>G	ENSP00000491591.1:n.*1338+1729A>G
ENST00000640816.1:n.1363-65A>G
ENST00000640888.2:c.955-65A>G MANE Select	ENSP00000492260.1:n.955-65A>G
ENST00000261434.7:c.955-65A>G	ENSP00000261434.3:n.955-65A>G
ENST00000340169.6:c.954+1729A>G	ENSP00000340676.2:n.954+1729A>G
ENST00000381846.1:c.826-65A>G	ENSP00000371270.1:n.826-65A>G
ENST00000513731.5:c.565-65A>G	ENSP00000425580.1:n.565-65A>G
NM_001278590.1:c.826-65A>G	NP_001265519.1:n.826-65A>G
NM_006859.3:c.955-65A>G	NP_006850.2:n.955-65A>G
NM_194451.2:c.954+1729A>G	NP_919433.1:n.954+1729A>G
XM_006713990.2:c.517-65A>G	XP_006714053.1:n.517-65A>G
NM_001363700.1:c.646-65A>G	NP_001350629.1:n.646-65A>G
XM_006713990.3:c.517-65A>G	XP_006714053.1:n.517-65A>G
XM_017007665.2:c.825+1729A>G	XP_016863154.1:n.825+1729A>G
XR_001741096.2:n.1694-65A>G
NM_001278590.2:c.826-65A>G	NP_001265519.1:n.826-65A>G
NM_001363700.2:c.646-65A>G	NP_001350629.1:n.646-65A>G
NM_006859.4:c.955-65A>G MANE Select	NP_006850.2:n.955-65A>G
NM_194451.3:c.954+1729A>G	NP_919433.1:n.954+1729A>G