Canonical Allele Identifier: CA2676320919
Gene: GABRA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.161848292_161848293insT , CM000667.2:g.161848292_161848293insT GRCh38
NC_000005.9:g.161275298_161275299insT , CM000667.1:g.161275298_161275299insT GRCh37
NC_000005.8:g.161207876_161207877insT NCBI36
NG_011548.1:g.6102_6103insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000393943.10:c.-146_-145insT MANE Select ENSP00000377517.4:n.-146_-145insT
ENST00000635916.2:n.630_631insT
ENST00000637044.1:c.-146_-145insT ENSP00000490684.1:n.-146_-145insT
ENST00000638112.1:c.-146_-145insT ENSP00000489839.1:n.-146_-145insT
ENST00000023897.10:c.-146_-145insT ENSP00000023897.6:n.-146_-145insT
ENST00000393943.9:c.-146_-145insT ENSP00000377517.4:n.-146_-145insT
ENST00000428797.7:c.-146_-145insT ENSP00000393097.2:n.-146_-145insT
ENST00000635096.1:c.-146_-145insT ENSP00000489033.1:n.-146_-145insT
NM_000806.5:c.-146_-145insT NP_000797.2:n.-146_-145insT
NM_001127643.1:c.-146_-145insT NP_001121115.1:n.-146_-145insT
NM_001127644.1:c.-146_-145insT NP_001121116.1:n.-146_-145insT
XR_941158.3:n.89+2227_89+2228insA
NM_001127644.2:c.-146_-145insT MANE Select NP_001121116.1:n.-146_-145insT
NM_001127643.2:c.-146_-145insT NP_001121115.1:n.-146_-145insT