Canonical Allele Identifier: CA2579461331

Gene: ENG

Linked Data

• gnomAD v4: 9-127825622-AGGGGGCGGGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127825627_127825636del , CM000671.2:g.127825627_127825636del	GRCh38
NC_000009.11:g.130587906_130587915del , CM000671.1:g.130587906_130587915del	GRCh37
NC_000009.10:g.129627727_129627736del	NCBI36
NG_009551.1:g.34137_34146del , LRG_589:g.34137_34146del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.143+63_143+72del	ENSP00000479015.1:n.143+63_143+72del
ENST00000373203.9:c.689+63_689+72del MANE Select	ENSP00000362299.4:n.689+63_689+72del
ENST00000344849.4:c.689+63_689+72del	ENSP00000341917.3:n.689+63_689+72del
ENST00000373203.8:c.689+63_689+72del	ENSP00000362299.4:n.689+63_689+72del
ENST00000480266.5:c.143+63_143+72del	ENSP00000479015.1:n.143+63_143+72del
NM_000118.3:c.689+63_689+72del , LRG_589t1:c.689+63_689+72del	NP_000109.1:n.689+63_689+72del
NM_001114753.2:c.689+63_689+72del , LRG_589t2:c.689+63_689+72del	NP_001108225.1:n.689+63_689+72del
NM_001278138.1:c.143+63_143+72del	NP_001265067.1:n.143+63_143+72del
XR_001746952.2:n.82+169_82+178del
NM_001114753.3:c.689+63_689+72del MANE Select	NP_001108225.1:n.689+63_689+72del
NM_001278138.2:c.143+63_143+72del	NP_001265067.1:n.143+63_143+72del