Canonical Allele Identifier: CA1596250014
Gene: GABRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.161848211A= , CM000667.2:g.161848211A= GRCh38
NC_000005.9:g.161275217A= , CM000667.1:g.161275217A= GRCh37
NC_000005.8:g.161207795A= NCBI36
NG_011548.1:g.6021A=

Transcript Alleles

HGVS Amino-acid change
ENST00000393943.10:c.-227A= MANE Select ENSP00000377517.4:n.-227A=
ENST00000635916.2:n.549A=
ENST00000638112.1:c.-227A= ENSP00000489839.1:n.-227A=
ENST00000023897.10:c.-227A= ENSP00000023897.6:n.-227A=
ENST00000393943.9:c.-227A= ENSP00000377517.4:n.-227A=
ENST00000428797.7:c.-227A= ENSP00000393097.2:n.-227A=
ENST00000635096.1:c.-227A= ENSP00000489033.1:n.-227A=
NM_000806.5:c.-227A= NP_000797.2:n.-227A=
NM_001127643.1:c.-227A= NP_001121115.1:n.-227A=
NM_001127644.1:c.-227A= NP_001121116.1:n.-227A=
XR_941158.3:n.89+2309T=
NM_001127644.2:c.-227A= MANE Select NP_001121116.1:n.-227A=
NM_001127643.2:c.-227A= NP_001121115.1:n.-227A=