Canonical Allele Identifier: CA362180120

Gene: GABRA1

Linked Data

• COSMIC: COSM736908
• MyVariant Identifiers: chr5:g.161322698A>T (hg19) ; chr5:g.161895692A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161895692A>T , CM000667.2:g.161895692A>T	GRCh38
NC_000005.9:g.161322698A>T , CM000667.1:g.161322698A>T	GRCh37
NC_000005.8:g.161255276A>T	NCBI36
NG_011548.1:g.53502A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000393943.10:c.883A>T MANE Select	ENSP00000377517.4:p.Thr295Ser
ENST00000635880.1:c.883A>T	ENSP00000489738.1:p.Thr295Ser
ENST00000635916.2:n.2484A>T
ENST00000636340.1:c.*732A>T	ENSP00000490002.1:n.*732A>T
ENST00000636408.1:n.687A>T
ENST00000636573.1:c.883A>T	ENSP00000490320.1:p.Thr295Ser
ENST00000637044.1:c.*657A>T	ENSP00000490684.1:n.*657A>T
ENST00000637827.1:c.883A>T	ENSP00000490804.1:p.Thr295Ser
ENST00000638112.1:c.883A>T	ENSP00000489839.1:p.Thr295Ser
ENST00000638159.1:c.928A>T	ENSP00000490360.1:p.Thr310Ser
ENST00000023897.10:c.883A>T	ENSP00000023897.6:p.Thr295Ser
ENST00000393943.9:c.883A>T	ENSP00000377517.4:p.Thr295Ser
ENST00000428797.7:c.883A>T	ENSP00000393097.2:p.Thr295Ser
ENST00000437025.6:c.883A>T	ENSP00000415441.2:p.Thr295Ser
NM_000806.5:c.883A>T	NP_000797.2:p.Thr295Ser
NM_001127643.1:c.883A>T	NP_001121115.1:p.Thr295Ser
NM_001127644.1:c.883A>T	NP_001121116.1:p.Thr295Ser
NM_001127645.1:c.883A>T	NP_001121117.1:p.Thr295Ser
NM_001127648.1:c.883A>T	NP_001121120.1:p.Thr295Ser
NM_001127644.2:c.883A>T MANE Select	NP_001121116.1:p.Thr295Ser
NM_001127643.2:c.883A>T	NP_001121115.1:p.Thr295Ser
NM_001127645.2:c.883A>T	NP_001121117.1:p.Thr295Ser
NM_001127648.2:c.883A>T	NP_001121120.1:p.Thr295Ser