Canonical Allele Identifier: CA2769177746
Gene: GABRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.161848278G>C , CM000667.2:g.161848278G>C GRCh38
NC_000005.9:g.161275284G>C , CM000667.1:g.161275284G>C GRCh37
NC_000005.8:g.161207862G>C NCBI36
NG_011548.1:g.6088G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000393943.10:c.-160G>C MANE Select ENSP00000377517.4:n.-160G>C
ENST00000635916.2:n.616G>C
ENST00000637044.1:c.-160G>C ENSP00000490684.1:n.-160G>C
ENST00000638112.1:c.-160G>C ENSP00000489839.1:n.-160G>C
ENST00000023897.10:c.-160G>C ENSP00000023897.6:n.-160G>C
ENST00000393943.9:c.-160G>C ENSP00000377517.4:n.-160G>C
ENST00000428797.7:c.-160G>C ENSP00000393097.2:n.-160G>C
ENST00000635096.1:c.-160G>C ENSP00000489033.1:n.-160G>C
NM_000806.5:c.-160G>C NP_000797.2:n.-160G>C
NM_001127643.1:c.-160G>C NP_001121115.1:n.-160G>C
NM_001127644.1:c.-160G>C NP_001121116.1:n.-160G>C
XR_941158.3:n.89+2242C>G
NM_001127644.2:c.-160G>C MANE Select NP_001121116.1:n.-160G>C
NM_001127643.2:c.-160G>C NP_001121115.1:n.-160G>C