Canonical Allele Identifier: CA447609857

Gene: GABRA1

Linked Data

• ClinVar Variation Id: 2947075
• ClinVar RCV Id: RCV003801265
• MyVariant Identifiers: chr5:g.161322721C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161895715C>T , CM000667.2:g.161895715C>T	GRCh38
NC_000005.9:g.161322721C>T , CM000667.1:g.161322721C>T	GRCh37
NC_000005.8:g.161255299C>T	NCBI36
NG_011548.1:g.53525C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000393943.10:c.906C>T MANE Select	ENSP00000377517.4:p.Asn302=
ENST00000635880.1:c.906C>T	ENSP00000489738.1:p.Asn302=
ENST00000635916.2:n.2507C>T
ENST00000636340.1:c.*755C>T	ENSP00000490002.1:n.*755C>T
ENST00000636408.1:n.710C>T
ENST00000636573.1:c.906C>T	ENSP00000490320.1:p.Asn302=
ENST00000637044.1:c.*680C>T	ENSP00000490684.1:n.*680C>T
ENST00000637827.1:c.906C>T	ENSP00000490804.1:p.Asn302=
ENST00000638112.1:c.906C>T	ENSP00000489839.1:p.Asn302=
ENST00000638159.1:c.951C>T	ENSP00000490360.1:p.Asn317=
ENST00000023897.10:c.906C>T	ENSP00000023897.6:p.Asn302=
ENST00000393943.9:c.906C>T	ENSP00000377517.4:p.Asn302=
ENST00000428797.7:c.906C>T	ENSP00000393097.2:p.Asn302=
ENST00000437025.6:c.906C>T	ENSP00000415441.2:p.Asn302=
NM_000806.5:c.906C>T	NP_000797.2:p.Asn302=
NM_001127643.1:c.906C>T	NP_001121115.1:p.Asn302=
NM_001127644.1:c.906C>T	NP_001121116.1:p.Asn302=
NM_001127645.1:c.906C>T	NP_001121117.1:p.Asn302=
NM_001127648.1:c.906C>T	NP_001121120.1:p.Asn302=
NM_001127644.2:c.906C>T MANE Select	NP_001121116.1:p.Asn302=
NM_001127643.2:c.906C>T	NP_001121115.1:p.Asn302=
NM_001127645.2:c.906C>T	NP_001121117.1:p.Asn302=
NM_001127648.2:c.906C>T	NP_001121120.1:p.Asn302=