Canonical Allele Identifier: CA374414887

Gene: ELP1

Linked Data

• MyVariant Identifiers: chr9:g.111651634A>C (hg19) ; chr9:g.108889354A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108889354A>C , CM000671.2:g.108889354A>C	GRCh38
NC_000009.11:g.111651634A>C , CM000671.1:g.111651634A>C	GRCh37
NC_000009.10:g.110691455A>C	NCBI36
NG_008788.1:g.49975T>G , LRG_251:g.49975T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374647.10:c.3200T>G MANE Select	ENSP00000363779.5:p.Met1067Arg
ENST00000495759.6:c.*1810T>G	ENSP00000433514.2:n.*1810T>G
ENST00000674535.1:c.3200T>G	ENSP00000502142.1:p.Met1067Arg
ENST00000674704.1:n.6285T>G
ENST00000674836.1:n.3813T>G
ENST00000674890.1:c.*435T>G	ENSP00000501870.1:n.*435T>G
ENST00000674938.1:c.2858T>G	ENSP00000502427.1:p.Met953Arg
ENST00000674948.1:c.2858T>G	ENSP00000501602.1:p.Met953Arg
ENST00000675052.1:c.3200T>G	ENSP00000502664.1:p.Met1067Arg
ENST00000675078.1:c.3200T>G	ENSP00000501549.1:p.Met1067Arg
ENST00000675215.1:c.*2424T>G	ENSP00000502558.1:n.*2424T>G
ENST00000675233.1:n.5027T>G
ENST00000675321.1:c.3200T>G	ENSP00000502751.1:p.Met1067Arg
ENST00000675325.1:n.5157T>G
ENST00000675335.1:c.3231T>G	ENSP00000502182.1:n.3231T>G
ENST00000675400.1:n.4935T>G
ENST00000675406.1:c.3200T>G	ENSP00000501893.1:p.Met1067Arg
ENST00000675458.1:c.3293T>G	ENSP00000501754.1:n.3293T>G
ENST00000675507.1:n.4996T>G
ENST00000675535.1:c.*827T>G	ENSP00000501667.1:n.*827T>G
ENST00000675566.1:n.5058T>G
ENST00000675602.1:n.6248T>G
ENST00000675647.1:n.4364T>G
ENST00000675711.1:c.3200T>G	ENSP00000502485.1:p.Met1067Arg
ENST00000675727.1:c.3200T>G	ENSP00000501722.1:p.Met1067Arg
ENST00000675748.1:n.4834T>G
ENST00000675765.1:c.*583T>G	ENSP00000502640.1:n.*583T>G
ENST00000675825.1:c.3200T>G	ENSP00000502632.1:p.Met1067Arg
ENST00000675877.1:n.3505T>G
ENST00000675893.1:c.*4269T>G	ENSP00000502001.1:n.*4269T>G
ENST00000675943.1:n.6815T>G
ENST00000675979.1:c.*2443T>G	ENSP00000502208.1:n.*2443T>G
ENST00000676044.1:c.*860T>G	ENSP00000502378.1:n.*860T>G
ENST00000676086.1:n.4985T>G
ENST00000676121.1:n.5028T>G
ENST00000676237.1:c.3101T>G	ENSP00000501828.1:p.Met1034Arg
ENST00000676416.1:c.2858T>G	ENSP00000501660.1:p.Met953Arg
ENST00000676424.1:n.4996T>G
ENST00000676429.1:n.7669T>G
ENST00000374647.9:c.3200T>G	ENSP00000363779.5:p.Met1067Arg
ENST00000467959.1:n.80T>G
ENST00000495759.5:c.340T>G
ENST00000537196.1:c.2153T>G	ENSP00000439367.1:p.Met718Arg
NM_003640.3:c.3200T>G , LRG_251t1:c.3200T>G	NP_003631.2:p.Met1067Arg
XM_005252285.2:c.2858T>G	XP_005252342.1:p.Met953Arg
XM_011519136.1:c.3200T>G	XP_011517438.1:p.Met1067Arg
XM_011519137.1:c.2858T>G	XP_011517439.1:p.Met953Arg
NM_001318360.1:c.2858T>G	NP_001305289.1:p.Met953Arg
NM_001330749.1:c.2153T>G	NP_001317678.1:p.Met718Arg
NM_003640.4:c.3200T>G	NP_003631.2:p.Met1067Arg
XM_011519136.2:c.3200T>G	XP_011517438.1:p.Met1067Arg
XR_929859.3:n.3589T>G
NM_003640.5:c.3200T>G MANE Select	NP_003631.2:p.Met1067Arg
NM_001318360.2:c.2858T>G	NP_001305289.1:p.Met953Arg
NM_001330749.2:c.2153T>G	NP_001317678.1:p.Met718Arg