Canonical Allele Identifier: CA447608920
Gene: GABRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.161300140A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.161873134A>T , CM000667.2:g.161873134A>T GRCh38
NC_000005.9:g.161300140A>T , CM000667.1:g.161300140A>T GRCh37
NC_000005.8:g.161232718A>T NCBI36
NG_011548.1:g.30944A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000393943.10:c.273A>T MANE Select ENSP00000377517.4:p.Val91=
ENST00000635880.1:c.273A>T ENSP00000489738.1:p.Val91=
ENST00000635916.2:n.1048A>T
ENST00000636340.1:c.*122A>T ENSP00000490002.1:n.*122A>T
ENST00000636408.1:n.77A>T
ENST00000636573.1:c.273A>T ENSP00000490320.1:p.Val91=
ENST00000637044.1:c.*47A>T ENSP00000490684.1:n.*47A>T
ENST00000637827.1:c.273A>T ENSP00000490804.1:p.Val91=
ENST00000638112.1:c.273A>T ENSP00000489839.1:p.Val91=
ENST00000638159.1:c.318A>T ENSP00000490360.1:p.Val106=
ENST00000023897.10:c.273A>T ENSP00000023897.6:p.Val91=
ENST00000393943.9:c.273A>T ENSP00000377517.4:p.Val91=
ENST00000428797.7:c.273A>T ENSP00000393097.2:p.Val91=
ENST00000437025.6:c.273A>T ENSP00000415441.2:p.Val91=
ENST00000519542.1:n.37A>T
ENST00000519621.2:c.273A>T ENSP00000430435.2:p.Val91=
ENST00000522651.6:c.336A>T ENSP00000430507.2:p.Val112=
ENST00000634335.1:c.273A>T ENSP00000489434.1:p.Val91=
NM_000806.5:c.273A>T NP_000797.2:p.Val91=
NM_001127643.1:c.273A>T NP_001121115.1:p.Val91=
NM_001127644.1:c.273A>T NP_001121116.1:p.Val91=
NM_001127645.1:c.273A>T NP_001121117.1:p.Val91=
NM_001127648.1:c.273A>T NP_001121120.1:p.Val91=
NM_001127644.2:c.273A>T MANE Select NP_001121116.1:p.Val91=
NM_001127643.2:c.273A>T NP_001121115.1:p.Val91=
NM_001127645.2:c.273A>T NP_001121117.1:p.Val91=
NM_001127648.2:c.273A>T NP_001121120.1:p.Val91=