Canonical Allele Identifier: CA2839401340

Gene: ELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74028132del , CM000669.2:g.74028132del	GRCh38
NC_000007.13:g.73442462del , CM000669.1:g.73442462del	GRCh37
NC_000007.12:g.73080398del	NCBI36
NG_009261.1:g.5036del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252034.11:c.-56del	ENSP00000252034.7:n.-56del
ENST00000320492.11:c.-56del	ENSP00000315607.7:n.-56del
ENST00000358929.8:c.-56del	ENSP00000351807.5:n.-56del
ENST00000414324.5:c.-56del	ENSP00000392575.1:n.-56del
ENST00000431562.5:c.-56del	ENSP00000394549.1:n.-56del
ENST00000438880.5:c.-56del	ENSP00000389206.1:n.-56del
ENST00000438906.5:c.-56del	ENSP00000406949.1:n.-56del
ENST00000445912.5:c.-56del	ENSP00000389857.1:n.-56del
ENST00000468517.5:n.7del
ENST00000492003.5:n.9del
ENST00000494160.5:n.19del
ENST00000621115.4:c.-56del	ENSP00000480955.1:n.-56del
NM_000501.3:c.-56del	NP_000492.2:n.-56del
NM_001081752.2:c.-56del	NP_001075221.1:n.-56del
NM_001081753.2:c.-56del	NP_001075222.1:n.-56del
NM_001081754.2:c.-56del	NP_001075223.1:n.-56del
NM_001081755.2:c.-56del	NP_001075224.1:n.-56del
NM_001278912.1:c.-56del	NP_001265841.1:n.-56del
NM_001278913.1:c.-56del	NP_001265842.1:n.-56del
NM_001278914.1:c.-56del	NP_001265843.1:n.-56del
NM_001278915.1:c.-56del	NP_001265844.1:n.-56del
NM_001278916.1:c.-56del	NP_001265845.1:n.-56del
NM_001278917.1:c.-56del	NP_001265846.1:n.-56del
NM_001278918.1:c.-56del	NP_001265847.1:n.-56del
NM_001278939.1:c.-56del	NP_001265868.1:n.-56del
XM_005250187.1:c.-56del	XP_005250244.1:n.-56del
XM_005250188.1:c.-56del	XP_005250245.1:n.-56del
XM_011515868.1:c.-56del	XP_011514170.1:n.-56del
XM_011515870.1:c.-56del	XP_011514172.1:n.-56del
XM_011515871.1:c.-56del	XP_011514173.1:n.-56del
XM_011515872.1:c.-56del	XP_011514174.1:n.-56del
XM_011515873.1:c.-56del	XP_011514175.1:n.-56del
XM_011515874.1:c.-56del	XP_011514176.1:n.-56del
XM_011515875.1:c.-56del	XP_011514177.1:n.-56del
XM_011515876.1:c.-56del	XP_011514178.1:n.-56del
XM_011515877.1:c.-56del	XP_011514179.1:n.-56del
XM_005250187.2:c.-56del	XP_005250244.1:n.-56del
XM_011515868.2:c.-56del	XP_011514170.1:n.-56del
XM_011515871.2:c.-56del	XP_011514173.1:n.-56del
XM_011515872.2:c.-56del	XP_011514174.1:n.-56del
XM_011515873.2:c.-56del	XP_011514175.1:n.-56del
XM_011515875.2:c.-56del	XP_011514177.1:n.-56del
XM_011515876.2:c.-56del	XP_011514178.1:n.-56del
XM_011515877.2:c.-56del	XP_011514179.1:n.-56del
XM_017011814.2:c.-56del	XP_016867303.1:n.-56del