Canonical Allele Identifier: CA356664911

Gene: LIAS

Linked Data

• MyVariant Identifiers: chr4:g.39469173A>C (hg19) ; chr4:g.39467553A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39467553A>C , CM000666.2:g.39467553A>C	GRCh38
NC_000004.11:g.39469173A>C , CM000666.1:g.39469173A>C	GRCh37
NC_000004.10:g.39145568A>C	NCBI36
NG_032111.1:g.13509A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261434.8:c.335A>C	ENSP00000261434.4:p.Asp112Ala
ENST00000340169.7:c.644A>C	ENSP00000340676.2:p.Asp215Ala
ENST00000381846.2:c.608+2211A>C	ENSP00000371270.1:n.608+2211A>C
ENST00000513731.6:c.254A>C	ENSP00000425580.1:p.Asp85Ala
ENST00000638422.1:c.644A>C	ENSP00000491001.1:p.Asp215Ala
ENST00000638430.1:c.341A>C
ENST00000638451.1:c.300-2466A>C	ENSP00000491681.1:n.300-2466A>C
ENST00000638816.1:c.358A>C	ENSP00000492482.1:n.358A>C
ENST00000639422.1:c.429A>C	ENSP00000491899.1:p.Ter143Cys
ENST00000640349.1:c.530A>C	ENSP00000491477.1:p.Asp177Ala
ENST00000640381.1:n.704A>C
ENST00000640672.1:c.368+2211A>C	ENSP00000492203.1:n.368+2211A>C
ENST00000640689.1:c.*247A>C	ENSP00000491591.1:n.*247A>C
ENST00000640888.2:c.644A>C MANE Select	ENSP00000492260.1:p.Asp215Ala
ENST00000261434.7:c.644A>C	ENSP00000261434.3:p.Asp215Ala
ENST00000340169.6:c.644A>C	ENSP00000340676.2:p.Asp215Ala
ENST00000381846.1:c.608+2211A>C	ENSP00000371270.1:n.608+2211A>C
ENST00000513731.5:c.254A>C	ENSP00000425580.1:p.Asp85Ala
NM_001278590.1:c.608+2211A>C	NP_001265519.1:n.608+2211A>C
NM_006859.3:c.644A>C	NP_006850.2:p.Asp215Ala
NM_194451.2:c.644A>C	NP_919433.1:p.Asp215Ala
XM_006713990.2:c.300-2466A>C	XP_006714053.1:n.300-2466A>C
NM_001363700.1:c.335A>C	NP_001350629.1:p.Asp112Ala
XM_006713990.3:c.300-2466A>C	XP_006714053.1:n.300-2466A>C
XM_017007665.2:c.608+2211A>C	XP_016863154.1:n.608+2211A>C
XR_001741096.2:n.732A>C
NM_001278590.2:c.608+2211A>C	NP_001265519.1:n.608+2211A>C
NM_001363700.2:c.335A>C	NP_001350629.1:p.Asp112Ala
NM_006859.4:c.644A>C MANE Select	NP_006850.2:p.Asp215Ala
NM_194451.3:c.644A>C	NP_919433.1:p.Asp215Ala