Canonical Allele Identifier: CA2676110953

Gene: GLRA1

Linked Data

• gnomAD v4: 5-151851383-G-GCAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151851383_151851384insCAGA , CM000667.2:g.151851383_151851384insCAGA	GRCh38
NC_000005.9:g.151230944_151230945insCAGA , CM000667.1:g.151230944_151230945insCAGA	GRCh37
NC_000005.8:g.151211137_151211138insCAGA	NCBI36
NG_011764.1:g.78453_78454insTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.912+6_912+7insTCTG MANE Select	ENSP00000274576.5:n.912+6_912+7insTCTG
ENST00000274576.8:c.912+6_912+7insTCTG	ENSP00000274576.4:n.912+6_912+7insTCTG
ENST00000455880.2:c.912+6_912+7insTCTG	ENSP00000411593.2:n.912+6_912+7insTCTG
ENST00000462581.6:c.*670+6_*670+7insTCTG	ENSP00000430595.1:n.*670+6_*670+7insTCTG
ENST00000471351.2:n.1195+6_1195+7insTCTG
NM_000171.3:c.912+6_912+7insTCTG	NP_000162.2:n.912+6_912+7insTCTG
NM_001146040.1:c.912+6_912+7insTCTG	NP_001139512.1:n.912+6_912+7insTCTG
NM_001292000.1:c.663+6_663+7insTCTG	NP_001278929.1:n.663+6_663+7insTCTG
XM_005268412.2:c.912+6_912+7insTCTG	XP_005268469.1:n.912+6_912+7insTCTG
NM_000171.4:c.912+6_912+7insTCTG MANE Select	NP_000162.2:n.912+6_912+7insTCTG
NM_001146040.2:c.912+6_912+7insTCTG	NP_001139512.1:n.912+6_912+7insTCTG
NM_001292000.2:c.663+6_663+7insTCTG	NP_001278929.1:n.663+6_663+7insTCTG