Canonical Allele Identifier: CA466673094

Gene: ELP1

Linked Data

• MyVariant Identifiers: chr9:g.111651657C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108889377C>T , CM000671.2:g.108889377C>T	GRCh38
NC_000009.11:g.111651657C>T , CM000671.1:g.111651657C>T	GRCh37
NC_000009.10:g.110691478C>T	NCBI36
NG_008788.1:g.49952G>A , LRG_251:g.49952G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374647.10:c.3177G>A MANE Select	ENSP00000363779.5:p.Gln1059=
ENST00000495759.6:c.*1787G>A	ENSP00000433514.2:n.*1787G>A
ENST00000674535.1:c.3177G>A	ENSP00000502142.1:p.Gln1059=
ENST00000674704.1:n.6262G>A
ENST00000674836.1:n.3790G>A
ENST00000674890.1:c.*412G>A	ENSP00000501870.1:n.*412G>A
ENST00000674938.1:c.2835G>A	ENSP00000502427.1:p.Gln945=
ENST00000674948.1:c.2835G>A	ENSP00000501602.1:p.Gln945=
ENST00000675052.1:c.3177G>A	ENSP00000502664.1:p.Gln1059=
ENST00000675078.1:c.3177G>A	ENSP00000501549.1:p.Gln1059=
ENST00000675215.1:c.*2401G>A	ENSP00000502558.1:n.*2401G>A
ENST00000675233.1:n.5004G>A
ENST00000675321.1:c.3177G>A	ENSP00000502751.1:p.Gln1059=
ENST00000675325.1:n.5134G>A
ENST00000675335.1:c.3208G>A	ENSP00000502182.1:n.3208G>A
ENST00000675400.1:n.4912G>A
ENST00000675406.1:c.3177G>A	ENSP00000501893.1:p.Gln1059=
ENST00000675458.1:c.3270G>A	ENSP00000501754.1:n.3270G>A
ENST00000675507.1:n.4973G>A
ENST00000675535.1:c.*804G>A	ENSP00000501667.1:n.*804G>A
ENST00000675566.1:n.5035G>A
ENST00000675602.1:n.6225G>A
ENST00000675647.1:n.4341G>A
ENST00000675711.1:c.3177G>A	ENSP00000502485.1:p.Gln1059=
ENST00000675727.1:c.3177G>A	ENSP00000501722.1:p.Gln1059=
ENST00000675748.1:n.4811G>A
ENST00000675765.1:c.*560G>A	ENSP00000502640.1:n.*560G>A
ENST00000675825.1:c.3177G>A	ENSP00000502632.1:p.Gln1059=
ENST00000675877.1:n.3482G>A
ENST00000675893.1:c.*4246G>A	ENSP00000502001.1:n.*4246G>A
ENST00000675943.1:n.6792G>A
ENST00000675979.1:c.*2420G>A	ENSP00000502208.1:n.*2420G>A
ENST00000676044.1:c.*837G>A	ENSP00000502378.1:n.*837G>A
ENST00000676086.1:n.4962G>A
ENST00000676121.1:n.5005G>A
ENST00000676237.1:c.3078G>A	ENSP00000501828.1:p.Gln1026=
ENST00000676416.1:c.2835G>A	ENSP00000501660.1:p.Gln945=
ENST00000676424.1:n.4973G>A
ENST00000676429.1:n.7646G>A
ENST00000374647.9:c.3177G>A	ENSP00000363779.5:p.Gln1059=
ENST00000467959.1:n.57G>A
ENST00000495759.5:c.317G>A
ENST00000537196.1:c.2130G>A	ENSP00000439367.1:p.Gln710=
NM_003640.3:c.3177G>A , LRG_251t1:c.3177G>A	NP_003631.2:p.Gln1059=
XM_005252285.2:c.2835G>A	XP_005252342.1:p.Gln945=
XM_011519136.1:c.3177G>A	XP_011517438.1:p.Gln1059=
XM_011519137.1:c.2835G>A	XP_011517439.1:p.Gln945=
NM_001318360.1:c.2835G>A	NP_001305289.1:p.Gln945=
NM_001330749.1:c.2130G>A	NP_001317678.1:p.Gln710=
NM_003640.4:c.3177G>A	NP_003631.2:p.Gln1059=
XM_011519136.2:c.3177G>A	XP_011517438.1:p.Gln1059=
XR_929859.3:n.3566G>A
NM_003640.5:c.3177G>A MANE Select	NP_003631.2:p.Gln1059=
NM_001318360.2:c.2835G>A	NP_001305289.1:p.Gln945=
NM_001330749.2:c.2130G>A	NP_001317678.1:p.Gln710=