Canonical Allele Identifier: CA2695211288

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127820043_127820044insAGCAAATGCTGGGT , CM000671.2:g.127820043_127820044insAGCAAATGCTGGGT	GRCh38
NC_000009.11:g.130582322_130582323insAGCAAATGCTGGGT , CM000671.1:g.130582322_130582323insAGCAAATGCTGGGT	GRCh37
NC_000009.10:g.129622143_129622144insAGCAAATGCTGGGT	NCBI36
NG_009551.1:g.39737_39738insCTACCCAGCATTTG , LRG_589:g.39737_39738insCTACCCAGCATTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.594_595insCTACCCAGCATTTG
ENST00000373203.9:c.1140_1141insCTACCCAGCATTTG
ENST00000344849.4:c.1140_1141insCTACCCAGCATTTG
ENST00000373203.8:c.1140_1141insCTACCCAGCATTTG
ENST00000480266.5:c.594_595insCTACCCAGCATTTG
ENST00000486329.1:n.108_109insCTACCCAGCATTTG
NM_000118.3:c.1140_1141insCTACCCAGCATTTG , LRG_589t1:c.1140_1141insCTACCCAGCATTTG
NM_001114753.2:c.1140_1141insCTACCCAGCATTTG , LRG_589t2:c.1140_1141insCTACCCAGCATTTG
NM_001278138.1:c.594_595insCTACCCAGCATTTG
NR_136302.1:n.1569-1152_1569-1151insAGCAAATGCTGGGT
NM_001114753.3:c.1140_1141insCTACCCAGCATTTG
NM_001278138.2:c.594_595insCTACCCAGCATTTG