Canonical Allele Identifier: CA2691112632

Gene: ELP1

Linked Data

• gnomAD v4: 9-108889406-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108889406T>C , CM000671.2:g.108889406T>C	GRCh38
NC_000009.11:g.111651686T>C , CM000671.1:g.111651686T>C	GRCh37
NC_000009.10:g.110691507T>C	NCBI36
NG_008788.1:g.49923A>G , LRG_251:g.49923A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374647.10:c.3161-13A>G MANE Select	ENSP00000363779.5:n.3161-13A>G
ENST00000495759.6:c.*1771-13A>G	ENSP00000433514.2:n.*1771-13A>G
ENST00000674535.1:c.3161-13A>G	ENSP00000502142.1:n.3161-13A>G
ENST00000674704.1:n.6246-13A>G
ENST00000674836.1:n.3774-13A>G
ENST00000674890.1:c.*396-13A>G	ENSP00000501870.1:n.*396-13A>G
ENST00000674938.1:c.2819-13A>G	ENSP00000502427.1:n.2819-13A>G
ENST00000674948.1:c.2819-13A>G	ENSP00000501602.1:n.2819-13A>G
ENST00000675052.1:c.3161-13A>G	ENSP00000502664.1:n.3161-13A>G
ENST00000675078.1:c.3161-13A>G	ENSP00000501549.1:n.3161-13A>G
ENST00000675215.1:c.*2385-13A>G	ENSP00000502558.1:n.*2385-13A>G
ENST00000675233.1:n.4988-13A>G
ENST00000675321.1:c.3161-13A>G	ENSP00000502751.1:n.3161-13A>G
ENST00000675325.1:n.5118-13A>G
ENST00000675335.1:c.3192-13A>G	ENSP00000502182.1:n.3192-13A>G
ENST00000675400.1:n.4896-13A>G
ENST00000675406.1:c.3161-13A>G	ENSP00000501893.1:n.3161-13A>G
ENST00000675458.1:c.3254-13A>G	ENSP00000501754.1:n.3254-13A>G
ENST00000675507.1:n.4957-13A>G
ENST00000675535.1:c.*788-13A>G	ENSP00000501667.1:n.*788-13A>G
ENST00000675566.1:n.5019-13A>G
ENST00000675602.1:n.6209-13A>G
ENST00000675647.1:n.4325-13A>G
ENST00000675711.1:c.3161-13A>G	ENSP00000502485.1:n.3161-13A>G
ENST00000675727.1:c.3161-13A>G	ENSP00000501722.1:n.3161-13A>G
ENST00000675748.1:n.4795-13A>G
ENST00000675765.1:c.*544-13A>G	ENSP00000502640.1:n.*544-13A>G
ENST00000675825.1:c.3161-13A>G	ENSP00000502632.1:n.3161-13A>G
ENST00000675877.1:n.3466-13A>G
ENST00000675893.1:c.*4230-13A>G	ENSP00000502001.1:n.*4230-13A>G
ENST00000675943.1:n.6776-13A>G
ENST00000675979.1:c.*2404-13A>G	ENSP00000502208.1:n.*2404-13A>G
ENST00000676044.1:c.*821-13A>G	ENSP00000502378.1:n.*821-13A>G
ENST00000676086.1:n.4946-13A>G
ENST00000676121.1:n.4989-13A>G
ENST00000676237.1:c.3062-13A>G	ENSP00000501828.1:n.3062-13A>G
ENST00000676416.1:c.2819-13A>G	ENSP00000501660.1:n.2819-13A>G
ENST00000676424.1:n.4957-13A>G
ENST00000676429.1:n.7630-13A>G
ENST00000374647.9:c.3161-13A>G	ENSP00000363779.5:n.3161-13A>G
ENST00000467959.1:n.41-13A>G
ENST00000495759.5:c.301-13A>G
ENST00000537196.1:c.2114-13A>G	ENSP00000439367.1:n.2114-13A>G
NM_003640.3:c.3161-13A>G , LRG_251t1:c.3161-13A>G	NP_003631.2:n.3161-13A>G
XM_005252285.2:c.2819-13A>G	XP_005252342.1:n.2819-13A>G
XM_011519136.1:c.3161-13A>G	XP_011517438.1:n.3161-13A>G
XM_011519137.1:c.2819-13A>G	XP_011517439.1:n.2819-13A>G
NM_001318360.1:c.2819-13A>G	NP_001305289.1:n.2819-13A>G
NM_001330749.1:c.2114-13A>G	NP_001317678.1:n.2114-13A>G
NM_003640.4:c.3161-13A>G	NP_003631.2:n.3161-13A>G
XM_011519136.2:c.3161-13A>G	XP_011517438.1:n.3161-13A>G
XR_929859.3:n.3550-13A>G
NM_003640.5:c.3161-13A>G MANE Select	NP_003631.2:n.3161-13A>G
NM_001318360.2:c.2819-13A>G	NP_001305289.1:n.2819-13A>G
NM_001330749.2:c.2114-13A>G	NP_001317678.1:n.2114-13A>G