Canonical Allele Identifier: CA1452162199
Gene: LIAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39467480C= , CM000666.2:g.39467480C= GRCh38
NC_000004.11:g.39469100C= , CM000666.1:g.39469100C= GRCh37
NC_000004.10:g.39145495C= NCBI36
NG_032111.1:g.13436C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261434.8:c.300-38C= ENSP00000261434.4:n.300-38C=
ENST00000340169.7:c.609-38C= ENSP00000340676.2:n.609-38C=
ENST00000381846.2:c.608+2138C= ENSP00000371270.1:n.608+2138C=
ENST00000513731.6:c.219-38C= ENSP00000425580.1:n.219-38C=
ENST00000638422.1:c.609-38C= ENSP00000491001.1:n.609-38C=
ENST00000638430.1:c.306-38C=
ENST00000638451.1:c.300-2539C= ENSP00000491681.1:n.300-2539C=
ENST00000638816.1:c.323-38C= ENSP00000492482.1:n.323-38C=
ENST00000639422.1:c.394-38C= ENSP00000491899.1:n.394-38C=
ENST00000640349.1:c.495-38C= ENSP00000491477.1:n.495-38C=
ENST00000640381.1:n.669-38C=
ENST00000640672.1:c.368+2138C= ENSP00000492203.1:n.368+2138C=
ENST00000640689.1:c.*212-38C= ENSP00000491591.1:n.*212-38C=
ENST00000640888.2:c.609-38C= MANE Select ENSP00000492260.1:n.609-38C=
ENST00000261434.7:c.609-38C= ENSP00000261434.3:n.609-38C=
ENST00000340169.6:c.609-38C= ENSP00000340676.2:n.609-38C=
ENST00000381846.1:c.608+2138C= ENSP00000371270.1:n.608+2138C=
ENST00000513731.5:c.219-38C= ENSP00000425580.1:n.219-38C=
NM_001278590.1:c.608+2138C= NP_001265519.1:n.608+2138C=
NM_006859.3:c.609-38C= NP_006850.2:n.609-38C=
NM_194451.2:c.609-38C= NP_919433.1:n.609-38C=
XM_006713990.2:c.300-2539C= XP_006714053.1:n.300-2539C=
NM_001363700.1:c.300-38C= NP_001350629.1:n.300-38C=
XM_006713990.3:c.300-2539C= XP_006714053.1:n.300-2539C=
XM_017007665.2:c.608+2138C= XP_016863154.1:n.608+2138C=
XR_001741096.2:n.697-38C=
NM_001278590.2:c.608+2138C= NP_001265519.1:n.608+2138C=
NM_001363700.2:c.300-38C= NP_001350629.1:n.300-38C=
NM_006859.4:c.609-38C= MANE Select NP_006850.2:n.609-38C=
NM_194451.3:c.609-38C= NP_919433.1:n.609-38C=