Canonical Allele Identifier: CA1871332999

Gene: ELP1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108889439C= , CM000671.2:g.108889439C=	GRCh38
NC_000009.11:g.111651719C= , CM000671.1:g.111651719C=	GRCh37
NC_000009.10:g.110691540C=	NCBI36
NG_008788.1:g.49890G= , LRG_251:g.49890G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374647.10:c.3161-46G= MANE Select	ENSP00000363779.5:n.3161-46G=
ENST00000495759.6:c.*1771-46G=	ENSP00000433514.2:n.*1771-46G=
ENST00000674535.1:c.3161-46G=	ENSP00000502142.1:n.3161-46G=
ENST00000674704.1:n.6246-46G=
ENST00000674836.1:n.3774-46G=
ENST00000674890.1:c.*396-46G=	ENSP00000501870.1:n.*396-46G=
ENST00000674938.1:c.2819-46G=	ENSP00000502427.1:n.2819-46G=
ENST00000674948.1:c.2819-46G=	ENSP00000501602.1:n.2819-46G=
ENST00000675052.1:c.3161-46G=	ENSP00000502664.1:n.3161-46G=
ENST00000675078.1:c.3161-46G=	ENSP00000501549.1:n.3161-46G=
ENST00000675215.1:c.*2385-46G=	ENSP00000502558.1:n.*2385-46G=
ENST00000675233.1:n.4988-46G=
ENST00000675321.1:c.3161-46G=	ENSP00000502751.1:n.3161-46G=
ENST00000675325.1:n.5118-46G=
ENST00000675335.1:c.3192-46G=	ENSP00000502182.1:n.3192-46G=
ENST00000675400.1:n.4896-46G=
ENST00000675406.1:c.3161-46G=	ENSP00000501893.1:n.3161-46G=
ENST00000675458.1:c.3254-46G=	ENSP00000501754.1:n.3254-46G=
ENST00000675507.1:n.4957-46G=
ENST00000675535.1:c.*788-46G=	ENSP00000501667.1:n.*788-46G=
ENST00000675566.1:n.5019-46G=
ENST00000675602.1:n.6209-46G=
ENST00000675647.1:n.4325-46G=
ENST00000675711.1:c.3161-46G=	ENSP00000502485.1:n.3161-46G=
ENST00000675727.1:c.3161-46G=	ENSP00000501722.1:n.3161-46G=
ENST00000675748.1:n.4795-46G=
ENST00000675765.1:c.*544-46G=	ENSP00000502640.1:n.*544-46G=
ENST00000675825.1:c.3161-46G=	ENSP00000502632.1:n.3161-46G=
ENST00000675877.1:n.3466-46G=
ENST00000675893.1:c.*4230-46G=	ENSP00000502001.1:n.*4230-46G=
ENST00000675943.1:n.6776-46G=
ENST00000675979.1:c.*2404-46G=	ENSP00000502208.1:n.*2404-46G=
ENST00000676044.1:c.*821-46G=	ENSP00000502378.1:n.*821-46G=
ENST00000676086.1:n.4946-46G=
ENST00000676121.1:n.4989-46G=
ENST00000676237.1:c.3062-46G=	ENSP00000501828.1:n.3062-46G=
ENST00000676416.1:c.2819-46G=	ENSP00000501660.1:n.2819-46G=
ENST00000676424.1:n.4957-46G=
ENST00000676429.1:n.7630-46G=
ENST00000374647.9:c.3161-46G=	ENSP00000363779.5:n.3161-46G=
ENST00000467959.1:n.41-46G=
ENST00000495759.5:c.301-46G=
ENST00000537196.1:c.2114-46G=	ENSP00000439367.1:n.2114-46G=
NM_003640.3:c.3161-46G= , LRG_251t1:c.3161-46G=	NP_003631.2:n.3161-46G=
XM_005252285.2:c.2819-46G=	XP_005252342.1:n.2819-46G=
XM_011519136.1:c.3161-46G=	XP_011517438.1:n.3161-46G=
XM_011519137.1:c.2819-46G=	XP_011517439.1:n.2819-46G=
NM_001318360.1:c.2819-46G=	NP_001305289.1:n.2819-46G=
NM_001330749.1:c.2114-46G=	NP_001317678.1:n.2114-46G=
NM_003640.4:c.3161-46G=	NP_003631.2:n.3161-46G=
XM_011519136.2:c.3161-46G=	XP_011517438.1:n.3161-46G=
XR_929859.3:n.3550-46G=
NM_003640.5:c.3161-46G= MANE Select	NP_003631.2:n.3161-46G=
NM_001318360.2:c.2819-46G=	NP_001305289.1:n.2819-46G=
NM_001330749.2:c.2114-46G=	NP_001317678.1:n.2114-46G=