Canonical Allele Identifier: CA1452162350
Gene: LIAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39467549C= , CM000666.2:g.39467549C= GRCh38
NC_000004.11:g.39469169C= , CM000666.1:g.39469169C= GRCh37
NC_000004.10:g.39145564C= NCBI36
NG_032111.1:g.13505C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261434.8:c.331C= ENSP00000261434.4:p.Pro111=
ENST00000340169.7:c.640C= ENSP00000340676.2:p.Pro214=
ENST00000381846.2:c.608+2207C= ENSP00000371270.1:n.608+2207C=
ENST00000513731.6:c.250C= ENSP00000425580.1:p.Pro84=
ENST00000638422.1:c.640C= ENSP00000491001.1:p.Pro214=
ENST00000638430.1:c.337C=
ENST00000638451.1:c.300-2470C= ENSP00000491681.1:n.300-2470C=
ENST00000638816.1:c.354C= ENSP00000492482.1:n.354C=
ENST00000639422.1:c.425C= ENSP00000491899.1:p.Ser142=
ENST00000640349.1:c.526C= ENSP00000491477.1:p.Pro176=
ENST00000640381.1:n.700C=
ENST00000640672.1:c.368+2207C= ENSP00000492203.1:n.368+2207C=
ENST00000640689.1:c.*243C= ENSP00000491591.1:n.*243C=
ENST00000640888.2:c.640C= MANE Select ENSP00000492260.1:p.Pro214=
ENST00000261434.7:c.640C= ENSP00000261434.3:p.Pro214=
ENST00000340169.6:c.640C= ENSP00000340676.2:p.Pro214=
ENST00000381846.1:c.608+2207C= ENSP00000371270.1:n.608+2207C=
ENST00000513731.5:c.250C= ENSP00000425580.1:p.Pro84=
NM_001278590.1:c.608+2207C= NP_001265519.1:n.608+2207C=
NM_006859.3:c.640C= NP_006850.2:p.Pro214=
NM_194451.2:c.640C= NP_919433.1:p.Pro214=
XM_006713990.2:c.300-2470C= XP_006714053.1:n.300-2470C=
NM_001363700.1:c.331C= NP_001350629.1:p.Pro111=
XM_006713990.3:c.300-2470C= XP_006714053.1:n.300-2470C=
XM_017007665.2:c.608+2207C= XP_016863154.1:n.608+2207C=
XR_001741096.2:n.728C=
NM_001278590.2:c.608+2207C= NP_001265519.1:n.608+2207C=
NM_001363700.2:c.331C= NP_001350629.1:p.Pro111=
NM_006859.4:c.640C= MANE Select NP_006850.2:p.Pro214=
NM_194451.3:c.640C= NP_919433.1:p.Pro214=