Canonical Allele Identifier: CA1452162407
Gene: LIAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39467562G= , CM000666.2:g.39467562G= GRCh38
NC_000004.11:g.39469182G= , CM000666.1:g.39469182G= GRCh37
NC_000004.10:g.39145577G= NCBI36
NG_032111.1:g.13518G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261434.8:c.344G= ENSP00000261434.4:p.Gly115=
ENST00000340169.7:c.653G= ENSP00000340676.2:p.Gly218=
ENST00000381846.2:c.608+2220G= ENSP00000371270.1:n.608+2220G=
ENST00000513731.6:c.263G= ENSP00000425580.1:p.Gly88=
ENST00000638422.1:c.653G= ENSP00000491001.1:p.Gly218=
ENST00000638430.1:c.350G=
ENST00000638451.1:c.300-2457G= ENSP00000491681.1:n.300-2457G=
ENST00000638816.1:c.367G= ENSP00000492482.1:n.367G=
ENST00000639422.1:c.*9G= ENSP00000491899.1:n.*9G=
ENST00000640349.1:c.539G= ENSP00000491477.1:p.Gly180=
ENST00000640381.1:n.713G=
ENST00000640672.1:c.368+2220G= ENSP00000492203.1:n.368+2220G=
ENST00000640689.1:c.*256G= ENSP00000491591.1:n.*256G=
ENST00000640888.2:c.653G= MANE Select ENSP00000492260.1:p.Gly218=
ENST00000261434.7:c.653G= ENSP00000261434.3:p.Gly218=
ENST00000340169.6:c.653G= ENSP00000340676.2:p.Gly218=
ENST00000381846.1:c.608+2220G= ENSP00000371270.1:n.608+2220G=
ENST00000513731.5:c.263G= ENSP00000425580.1:p.Gly88=
NM_001278590.1:c.608+2220G= NP_001265519.1:n.608+2220G=
NM_006859.3:c.653G= NP_006850.2:p.Gly218=
NM_194451.2:c.653G= NP_919433.1:p.Gly218=
XM_006713990.2:c.300-2457G= XP_006714053.1:n.300-2457G=
NM_001363700.1:c.344G= NP_001350629.1:p.Gly115=
XM_006713990.3:c.300-2457G= XP_006714053.1:n.300-2457G=
XM_017007665.2:c.608+2220G= XP_016863154.1:n.608+2220G=
XR_001741096.2:n.741G=
NM_001278590.2:c.608+2220G= NP_001265519.1:n.608+2220G=
NM_001363700.2:c.344G= NP_001350629.1:p.Gly115=
NM_006859.4:c.653G= MANE Select NP_006850.2:p.Gly218=
NM_194451.3:c.653G= NP_919433.1:p.Gly218=