Canonical Allele Identifier: CA1596250023
Gene: GABRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.161848225T= , CM000667.2:g.161848225T= GRCh38
NC_000005.9:g.161275231T= , CM000667.1:g.161275231T= GRCh37
NC_000005.8:g.161207809T= NCBI36
NG_011548.1:g.6035T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393943.10:c.-213T= MANE Select ENSP00000377517.4:n.-213T=
ENST00000635916.2:n.563T=
ENST00000638112.1:c.-213T= ENSP00000489839.1:n.-213T=
ENST00000023897.10:c.-213T= ENSP00000023897.6:n.-213T=
ENST00000393943.9:c.-213T= ENSP00000377517.4:n.-213T=
ENST00000428797.7:c.-213T= ENSP00000393097.2:n.-213T=
ENST00000635096.1:c.-213T= ENSP00000489033.1:n.-213T=
NM_000806.5:c.-213T= NP_000797.2:n.-213T=
NM_001127643.1:c.-213T= NP_001121115.1:n.-213T=
NM_001127644.1:c.-213T= NP_001121116.1:n.-213T=
XR_941158.3:n.89+2295A=
NM_001127644.2:c.-213T= MANE Select NP_001121116.1:n.-213T=
NM_001127643.2:c.-213T= NP_001121115.1:n.-213T=