Canonical Allele Identifier: CA342791923

Gene: GON4L

Linked Data

• ClinVar Variation Id: 487779
• ClinVar RCV Id: RCV000577846
• dbSNP Id: rs1553200563
• MyVariant Identifiers: chr1:g.155742897T>C (hg19) ; chr1:g.155773106T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155773106T>C , CM000663.2:g.155773106T>C	GRCh38
NC_000001.10:g.155742897T>C , CM000663.1:g.155742897T>C	GRCh37
NC_000001.9:g.154009521T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622608.2:c.2455A>G	ENSP00000478593.2:p.Asn819Asp
ENST00000368331.6:c.2455A>G MANE Select	ENSP00000357315.1:p.Asn819Asp
ENST00000271883.9:c.2455A>G	ENSP00000271883.5:p.Asn819Asp
ENST00000361040.9:c.2455A>G	ENSP00000354322.5:p.Asn819Asp
ENST00000368331.5:c.2455A>G	ENSP00000357315.1:p.Asn819Asp
ENST00000437809.5:c.2455A>G	ENSP00000396117.1:p.Asn819Asp
ENST00000471341.5:n.2863A>G
ENST00000490801.1:n.383A>G
ENST00000497369.5:n.315A>G
ENST00000615926.4:c.2455A>G	ENSP00000483100.1:p.Asn819Asp
ENST00000620426.4:c.2455A>G	ENSP00000481460.1:p.Asn819Asp
ENST00000622608.1:c.2455A>G	ENSP00000478593.1:p.Asn819Asp
NM_001282856.1:c.2455A>G	NP_001269785.1:p.Asn819Asp
NM_001282858.1:c.2455A>G	NP_001269787.1:p.Asn819Asp
NM_001282860.1:c.2455A>G	NP_001269789.1:p.Asn819Asp
NM_001282861.1:c.2455A>G	NP_001269790.1:p.Asn819Asp
NM_032292.5:c.2455A>G	NP_115668.4:p.Asn819Asp
XM_005245284.2:c.1939A>G	XP_005245341.1:p.Asn647Asp
XM_005245286.2:c.43A>G	XP_005245343.1:p.Asn15Asp
XM_006711393.2:c.2455A>G	XP_006711456.1:p.Asn819Asp
XM_006711394.2:c.2455A>G	XP_006711457.1:p.Asn819Asp
XM_006711396.2:c.2455A>G	XP_006711459.1:p.Asn819Asp
XM_011509658.1:c.2368A>G	XP_011507960.1:p.Asn790Asp
XM_011509659.1:c.1939A>G	XP_011507961.1:p.Asn647Asp
XM_005245284.3:c.1939A>G	XP_005245341.1:p.Asn647Asp
XM_005245286.3:c.43A>G	XP_005245343.1:p.Asn15Asp
XM_006711393.3:c.2455A>G	XP_006711456.1:p.Asn819Asp
XM_006711394.4:c.2455A>G	XP_006711457.1:p.Asn819Asp
XM_011509658.2:c.2368A>G	XP_011507960.1:p.Asn790Asp
XM_011509659.2:c.1939A>G	XP_011507961.1:p.Asn647Asp
NM_001282858.2:c.2455A>G	NP_001269787.1:p.Asn819Asp
NM_001282860.2:c.2455A>G MANE Select	NP_001269789.1:p.Asn819Asp
NM_001282861.2:c.2455A>G	NP_001269790.1:p.Asn819Asp
NM_032292.6:c.2455A>G	NP_115668.4:p.Asn819Asp
NM_001282856.2:c.2455A>G	NP_001269785.1:p.Asn819Asp