Canonical Allele Identifier: CA1596250013
Gene: GABRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1757281702

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.161848209G>A , CM000667.2:g.161848209G>A GRCh38
NC_000005.9:g.161275215G>A , CM000667.1:g.161275215G>A GRCh37
NC_000005.8:g.161207793G>A NCBI36
NG_011548.1:g.6019G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000393943.10:c.-229G>A MANE Select ENSP00000377517.4:n.-229G>A
ENST00000635916.2:n.547G>A
ENST00000638112.1:c.-229G>A ENSP00000489839.1:n.-229G>A
ENST00000023897.10:c.-229G>A ENSP00000023897.6:n.-229G>A
ENST00000393943.9:c.-229G>A ENSP00000377517.4:n.-229G>A
ENST00000428797.7:c.-229G>A ENSP00000393097.2:n.-229G>A
ENST00000635096.1:c.-229G>A ENSP00000489033.1:n.-229G>A
NM_000806.5:c.-229G>A NP_000797.2:n.-229G>A
NM_001127643.1:c.-229G>A NP_001121115.1:n.-229G>A
NM_001127644.1:c.-229G>A NP_001121116.1:n.-229G>A
XR_941158.3:n.89+2311C>T
NM_001127644.2:c.-229G>A MANE Select NP_001121116.1:n.-229G>A
NM_001127643.2:c.-229G>A NP_001121115.1:n.-229G>A