Canonical Allele Identifier: CA12174862
Gene: GABRA1 HGNC NCBI

Linked Data

dbSNP Id: rs6883877

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.161851332C>T , CM000667.2:g.161851332C>T GRCh38
NC_000005.9:g.161278338C>T , CM000667.1:g.161278338C>T GRCh37
NC_000005.8:g.161210916C>T NCBI36
NG_011548.1:g.9142C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000393943.10:c.74+448C>T MANE Select ENSP00000377517.4:p.=
ENST00000635880.1:c.74+448C>T ENSP00000489738.1:p.=
ENST00000636340.1:c.74+448C>T ENSP00000490002.1:p.=
ENST00000636573.1:c.74+448C>T ENSP00000490320.1:p.=
ENST00000637044.1:c.74+448C>T ENSP00000490684.1:p.=
ENST00000637827.1:c.74+448C>T ENSP00000490804.1:p.=
ENST00000638112.1:c.74+448C>T ENSP00000489839.1:p.=
ENST00000638159.1:c.119+448C>T ENSP00000490360.1:p.=
ENST00000023897.10:c.74+448C>T ENSP00000023897.6:p.=
ENST00000393943.9:c.74+448C>T ENSP00000377517.4:p.=
ENST00000428797.7:c.74+448C>T ENSP00000393097.2:p.=
ENST00000437025.6:c.74+448C>T ENSP00000415441.2:p.=
ENST00000519621.2:c.74+448C>T ENSP00000430435.2:p.=
ENST00000521339.5:c.92+448C>T ENSP00000430895.1:p.=
ENST00000522651.6:c.137+448C>T ENSP00000430507.2:p.=
ENST00000634335.1:c.74+448C>T ENSP00000489434.1:p.=
ENST00000635096.1:c.74+448C>T ENSP00000489033.1:p.=
NM_000806.5:c.74+448C>T NP_000797.2:p.=
NM_001127643.1:c.74+448C>T NP_001121115.1:p.=
NM_001127644.1:c.74+448C>T NP_001121116.1:p.=
NM_001127645.1:c.74+448C>T NP_001121117.1:p.=
NM_001127648.1:c.74+448C>T NP_001121120.1:p.=
NM_001127644.2:c.74+448C>T MANE Select NP_001121116.1:p.=
NM_001127643.2:c.74+448C>T NP_001121115.1:p.=
NM_001127645.2:c.74+448C>T NP_001121117.1:p.=
NM_001127648.2:c.74+448C>T NP_001121120.1:p.=