Canonical Allele Identifier: CA1596250032
Gene: GABRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.161848245C= , CM000667.2:g.161848245C= GRCh38
NC_000005.9:g.161275251C= , CM000667.1:g.161275251C= GRCh37
NC_000005.8:g.161207829C= NCBI36
NG_011548.1:g.6055C=

Transcript Alleles

HGVS Amino-acid change
ENST00000393943.10:c.-193C= MANE Select ENSP00000377517.4:n.-193C=
ENST00000635916.2:n.583C=
ENST00000638112.1:c.-193C= ENSP00000489839.1:n.-193C=
ENST00000023897.10:c.-193C= ENSP00000023897.6:n.-193C=
ENST00000393943.9:c.-193C= ENSP00000377517.4:n.-193C=
ENST00000428797.7:c.-193C= ENSP00000393097.2:n.-193C=
ENST00000635096.1:c.-193C= ENSP00000489033.1:n.-193C=
NM_000806.5:c.-193C= NP_000797.2:n.-193C=
NM_001127643.1:c.-193C= NP_001121115.1:n.-193C=
NM_001127644.1:c.-193C= NP_001121116.1:n.-193C=
XR_941158.3:n.89+2275G=
NM_001127644.2:c.-193C= MANE Select NP_001121116.1:n.-193C=
NM_001127643.2:c.-193C= NP_001121115.1:n.-193C=