Canonical Allele Identifier: CA438944842

Gene: LIAS

Linked Data

• MyVariant Identifiers: chr4:g.39462538C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39460918C>G , CM000666.2:g.39460918C>G	GRCh38
NC_000004.11:g.39462538C>G , CM000666.1:g.39462538C>G	GRCh37
NC_000004.10:g.39138933C>G	NCBI36
NG_032111.1:g.6874C>G
NG_052985.1:g.3031G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261434.8:c.174C>G	ENSP00000261434.4:p.Thr58=
ENST00000340169.7:c.174C>G	ENSP00000340676.2:p.Thr58=
ENST00000381846.2:c.174C>G	ENSP00000371270.1:p.Thr58=
ENST00000513731.6:c.174C>G	ENSP00000425580.1:p.Thr58=
ENST00000638422.1:c.174C>G	ENSP00000491001.1:p.Thr58=
ENST00000638430.1:c.46C>G
ENST00000638451.1:c.174C>G	ENSP00000491681.1:p.Thr58=
ENST00000638816.1:c.45C>G	ENSP00000492482.1:p.Thr15=
ENST00000638837.1:c.174C>G	ENSP00000492038.1:p.Thr58=
ENST00000639422.1:c.174C>G	ENSP00000491899.1:p.Thr58=
ENST00000640349.1:c.174C>G	ENSP00000491477.1:p.Thr58=
ENST00000640381.1:n.234C>G
ENST00000640489.1:c.*73C>G	ENSP00000492540.1:n.*73C>G
ENST00000640689.1:c.174C>G	ENSP00000491591.1:p.Thr58=
ENST00000640888.2:c.174C>G MANE Select	ENSP00000492260.1:p.Thr58=
ENST00000261434.7:c.174C>G	ENSP00000261434.3:p.Thr58=
ENST00000340169.6:c.174C>G	ENSP00000340676.2:p.Thr58=
ENST00000381846.1:c.174C>G	ENSP00000371270.1:p.Thr58=
ENST00000424936.6:n.234C>G
ENST00000509519.5:n.247C>G
ENST00000513731.5:c.174C>G	ENSP00000425580.1:p.Thr58=
ENST00000515061.1:n.172C>G
NM_001278590.1:c.174C>G	NP_001265519.1:p.Thr58=
NM_001278591.1:c.174C>G	NP_001265520.1:p.Thr58=
NM_001278592.1:c.174C>G	NP_001265521.1:p.Thr58=
NM_006859.3:c.174C>G	NP_006850.2:p.Thr58=
NM_194451.2:c.174C>G	NP_919433.1:p.Thr58=
XM_006713990.2:c.174C>G	XP_006714053.1:p.Thr58=
NM_001363700.1:c.174C>G	NP_001350629.1:p.Thr58=
XM_006713990.3:c.174C>G	XP_006714053.1:p.Thr58=
XM_017007665.2:c.174C>G	XP_016863154.1:p.Thr58=
XR_001741096.2:n.262C>G
NM_001278590.2:c.174C>G	NP_001265519.1:p.Thr58=
NM_001363700.2:c.174C>G	NP_001350629.1:p.Thr58=
NM_006859.4:c.174C>G MANE Select	NP_006850.2:p.Thr58=
NM_194451.3:c.174C>G	NP_919433.1:p.Thr58=
NM_001278591.2:c.174C>G	NP_001265520.1:p.Thr58=
NM_001278592.2:c.174C>G	NP_001265521.1:p.Thr58=