Canonical Allele Identifier: CA1596250068
Gene: GABRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.161848297C= , CM000667.2:g.161848297C= GRCh38
NC_000005.9:g.161275303C= , CM000667.1:g.161275303C= GRCh37
NC_000005.8:g.161207881C= NCBI36
NG_011548.1:g.6107C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393943.10:c.-141C= MANE Select ENSP00000377517.4:n.-141C=
ENST00000635916.2:n.635C=
ENST00000637044.1:c.-141C= ENSP00000490684.1:n.-141C=
ENST00000638112.1:c.-141C= ENSP00000489839.1:n.-141C=
ENST00000023897.10:c.-141C= ENSP00000023897.6:n.-141C=
ENST00000393943.9:c.-141C= ENSP00000377517.4:n.-141C=
ENST00000428797.7:c.-141C= ENSP00000393097.2:n.-141C=
ENST00000635096.1:c.-141C= ENSP00000489033.1:n.-141C=
NM_000806.5:c.-141C= NP_000797.2:n.-141C=
NM_001127643.1:c.-141C= NP_001121115.1:n.-141C=
NM_001127644.1:c.-141C= NP_001121116.1:n.-141C=
XR_941158.3:n.89+2223G=
NM_001127644.2:c.-141C= MANE Select NP_001121116.1:n.-141C=
NM_001127643.2:c.-141C= NP_001121115.1:n.-141C=