Canonical Allele Identifier: CA1879973390

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824807_127824808delinsGG , CM000671.2:g.127824807_127824808delinsGG	GRCh38
NC_000009.11:g.130587086_130587087delinsGG , CM000671.1:g.130587086_130587087delinsGG	GRCh37
NC_000009.10:g.129626907_129626908delinsGG	NCBI36
NG_009551.1:g.34961_34962delinsCC , LRG_589:g.34961_34962delinsCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.437_438delinsCC	ENSP00000479015.1:p.Ser146=
ENST00000373203.9:c.983_984delinsCC MANE Select	ENSP00000362299.4:p.Ser328=
ENST00000344849.4:c.983_984delinsCC	ENSP00000341917.3:p.Ser328=
ENST00000373203.8:c.983_984delinsCC	ENSP00000362299.4:p.Ser328=
ENST00000480266.5:c.437_438delinsCC	ENSP00000479015.1:p.Ser146=
NM_000118.3:c.983_984delinsCC , LRG_589t1:c.983_984delinsCC	NP_000109.1:p.Ser328=
NM_001114753.2:c.983_984delinsCC , LRG_589t2:c.983_984delinsCC	NP_001108225.1:p.Ser328=
NM_001278138.1:c.437_438delinsCC	NP_001265067.1:p.Ser146=
NM_001114753.3:c.983_984delinsCC MANE Select	NP_001108225.1:p.Ser328=
NM_001278138.2:c.437_438delinsCC	NP_001265067.1:p.Ser146=