Canonical Allele Identifier: CA2656330560

Gene: LARGE1

Linked Data

• gnomAD v4: 22-33304653-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.33304656del , CM000684.2:g.33304656del	GRCh38
NC_000022.10:g.33700642del , CM000684.1:g.33700642del	GRCh37
NC_000022.9:g.32030642del	NCBI36
NG_009929.2:g.620775del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354992.7:c.1452-147del	ENSP00000347088.2:n.1452-147del
ENST00000397394.8:c.1452-147del MANE Select	ENSP00000380549.2:n.1452-147del
ENST00000402320.6:c.1296-147del	ENSP00000385223.1:n.1296-147del
ENST00000413114.6:c.1452-147del	ENSP00000415546.2:n.1452-147del
ENST00000608642.6:c.1452-147del	ENSP00000476866.2:n.1452-147del
ENST00000609799.6:c.1451+11431del	ENSP00000476415.2:n.1451+11431del
ENST00000610186.6:c.1452-147del	ENSP00000476364.2:n.1452-147del
ENST00000674543.1:c.1452-147del	ENSP00000501590.1:n.1452-147del
ENST00000674668.1:c.1326-147del	ENSP00000502103.1:n.1326-147del
ENST00000674708.1:n.1110-147del
ENST00000674780.1:c.849-147del	ENSP00000502772.1:n.849-147del
ENST00000674789.1:c.1452-147del	ENSP00000501941.1:n.1452-147del
ENST00000674816.1:n.1260-147del
ENST00000674999.1:c.1248-147del	ENSP00000502711.1:n.1248-147del
ENST00000675277.1:c.1248-147del	ENSP00000502702.1:n.1248-147del
ENST00000675382.1:c.1288-147del	ENSP00000501800.1:n.1288-147del
ENST00000675416.1:c.1452-147del	ENSP00000502826.1:n.1452-147del
ENST00000676031.1:c.*34-147del	ENSP00000501663.1:n.*34-147del
ENST00000676070.1:c.1452-147del	ENSP00000502152.1:n.1452-147del
ENST00000676126.1:c.1451+11431del	ENSP00000501966.1:n.1451+11431del
ENST00000676132.1:c.1452-147del	ENSP00000501854.1:n.1452-147del
ENST00000676370.1:c.1452-147del	ENSP00000502238.1:n.1452-147del
ENST00000354992.6:c.1452-147del	ENSP00000347088.2:n.1452-147del
ENST00000397394.6:c.1452-147del	ENSP00000380549.2:n.1452-147del
ENST00000402320.5:c.1296-147del	ENSP00000385223.1:n.1296-147del
ENST00000608642.5:c.483-147del	ENSP00000476866.1:n.483-147del
ENST00000609799.5:c.482+11431del	ENSP00000476415.1:n.482+11431del
ENST00000610186.5:c.483-147del	ENSP00000476364.1:n.483-147del
NM_004737.4:c.1452-147del	NP_004728.1:n.1452-147del
NM_133642.3:c.1452-147del	NP_598397.1:n.1452-147del
XM_005261831.2:c.1452-147del	XP_005261888.1:n.1452-147del
XM_005261832.2:c.1452-147del	XP_005261889.1:n.1452-147del
XM_011530510.1:c.1452-147del	XP_011528812.1:n.1452-147del
XM_011530511.1:c.1451+11431del	XP_011528813.1:n.1451+11431del
XM_011530512.1:c.849-147del	XP_011528814.1:n.849-147del
XM_011530513.1:c.354-147del	XP_011528815.1:n.354-147del
NM_001362949.1:c.1452-147del	NP_001349878.1:n.1452-147del
NM_001362951.1:c.1452-147del	NP_001349880.1:n.1452-147del
NM_001362953.1:c.1452-147del	NP_001349882.1:n.1452-147del
NM_004737.6:c.1452-147del	NP_004728.1:n.1452-147del
NM_133642.4:c.1452-147del	NP_598397.1:n.1452-147del
XM_005261831.3:c.1452-147del	XP_005261888.1:n.1452-147del
XM_005261832.3:c.1452-147del	XP_005261889.1:n.1452-147del
XM_011530512.2:c.849-147del	XP_011528814.1:n.849-147del
XM_011530513.2:c.354-147del	XP_011528815.1:n.354-147del
XM_024452302.1:c.1452-147del	XP_024308070.1:n.1452-147del
XR_002958722.1:n.1499-147del
NM_001362949.2:c.1452-147del	NP_001349878.1:n.1452-147del
NM_001362951.2:c.1452-147del	NP_001349880.1:n.1452-147del
NM_001362953.2:c.1452-147del	NP_001349882.1:n.1452-147del
NM_001378624.1:c.1452-147del	NP_001365553.1:n.1452-147del
NM_001378625.1:c.1452-147del	NP_001365554.1:n.1452-147del
NM_001378626.1:c.1452-147del	NP_001365555.1:n.1452-147del
NM_001378627.1:c.1452-147del	NP_001365556.1:n.1452-147del
NM_001378628.1:c.1452-147del	NP_001365557.1:n.1452-147del
NM_001378629.1:c.1296-147del	NP_001365558.1:n.1296-147del
NM_001378630.1:c.849-147del	NP_001365559.1:n.849-147del
NM_001378631.1:c.693-147del	NP_001365560.1:n.693-147del
NM_004737.7:c.1452-147del	NP_004728.1:n.1452-147del
NM_133642.5:c.1452-147del MANE Select	NP_598397.1:n.1452-147del