Canonical Allele Identifier: CA1596250054
Gene: GABRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.161848279T= , CM000667.2:g.161848279T= GRCh38
NC_000005.9:g.161275285T= , CM000667.1:g.161275285T= GRCh37
NC_000005.8:g.161207863T= NCBI36
NG_011548.1:g.6089T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393943.10:c.-159T= MANE Select ENSP00000377517.4:n.-159T=
ENST00000635916.2:n.617T=
ENST00000637044.1:c.-159T= ENSP00000490684.1:n.-159T=
ENST00000638112.1:c.-159T= ENSP00000489839.1:n.-159T=
ENST00000023897.10:c.-159T= ENSP00000023897.6:n.-159T=
ENST00000393943.9:c.-159T= ENSP00000377517.4:n.-159T=
ENST00000428797.7:c.-159T= ENSP00000393097.2:n.-159T=
ENST00000635096.1:c.-159T= ENSP00000489033.1:n.-159T=
NM_000806.5:c.-159T= NP_000797.2:n.-159T=
NM_001127643.1:c.-159T= NP_001121115.1:n.-159T=
NM_001127644.1:c.-159T= NP_001121116.1:n.-159T=
XR_941158.3:n.89+2241A=
NM_001127644.2:c.-159T= MANE Select NP_001121116.1:n.-159T=
NM_001127643.2:c.-159T= NP_001121115.1:n.-159T=