Canonical Allele Identifier: CA1879990314

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127820208_127820212delinsCTTTT , CM000671.2:g.127820208_127820212delinsCTTTT	GRCh38
NC_000009.11:g.130582487_130582491delinsCTTTT , CM000671.1:g.130582487_130582491delinsCTTTT	GRCh37
NC_000009.10:g.129622308_129622312delinsCTTTT	NCBI36
NG_009551.1:g.39557_39561delinsAAAAG , LRG_589:g.39557_39561delinsAAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.589-175_589-171delinsAAAAG	ENSP00000479015.1:n.589-175_589-171delinsAAAAG
ENST00000373203.9:c.1135-175_1135-171delinsAAAAG MANE Select	ENSP00000362299.4:n.1135-175_1135-171delinsAAAAG
ENST00000344849.4:c.1135-175_1135-171delinsAAAAG	ENSP00000341917.3:n.1135-175_1135-171delinsAAAAG
ENST00000373203.8:c.1135-175_1135-171delinsAAAAG	ENSP00000362299.4:n.1135-175_1135-171delinsAAAAG
ENST00000480266.5:c.589-175_589-171delinsAAAAG	ENSP00000479015.1:n.589-175_589-171delinsAAAAG
ENST00000486329.1:n.103-175_103-171delinsAAAAG
NM_000118.3:c.1135-175_1135-171delinsAAAAG , LRG_589t1:c.1135-175_1135-171delinsAAAAG	NP_000109.1:n.1135-175_1135-171delinsAAAAG
NM_001114753.2:c.1135-175_1135-171delinsAAAAG , LRG_589t2:c.1135-175_1135-171delinsAAAAG	NP_001108225.1:n.1135-175_1135-171delinsAAAAG
NM_001278138.1:c.589-175_589-171delinsAAAAG	NP_001265067.1:n.589-175_589-171delinsAAAAG
NR_136302.1:n.1569-987_1569-983delinsCTTTT
NM_001114753.3:c.1135-175_1135-171delinsAAAAG MANE Select	NP_001108225.1:n.1135-175_1135-171delinsAAAAG
NM_001278138.2:c.589-175_589-171delinsAAAAG	NP_001265067.1:n.589-175_589-171delinsAAAAG