Canonical Allele Identifier: CA362184263

Gene: GABRG2

Linked Data

• COSMIC: COSM3776487
• MyVariant Identifiers: chr5:g.161580368C>A (hg19) ; chr5:g.162153362C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153362C>A , CM000667.2:g.162153362C>A	GRCh38
NC_000005.9:g.161580368C>A , CM000667.1:g.161580368C>A	GRCh37
NC_000005.8:g.161512946C>A	NCBI36
NG_009290.1:g.90721C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1423C>A
ENST00000361925.9:c.1518C>A	ENSP00000354651.5:p.Tyr506Ter
ENST00000523372.2:c.1481C>A
ENST00000638253.1:n.676C>A
ENST00000638552.1:c.1113C>A	ENSP00000491763.1:p.Tyr371Ter
ENST00000638660.1:c.1137C>A	ENSP00000492869.1:p.Tyr379Ter
ENST00000638772.1:c.*4019C>A	ENSP00000491557.1:n.*4019C>A
ENST00000638877.1:c.1299C>A
ENST00000639046.1:c.789C>A	ENSP00000492659.1:p.Tyr263Ter
ENST00000639111.2:c.1398C>A	ENSP00000492125.2:p.Tyr466Ter
ENST00000639213.2:c.1422C>A MANE Select	ENSP00000491909.2:p.Tyr474Ter
ENST00000639278.1:c.2085C>A	ENSP00000491958.1:n.2085C>A
ENST00000639384.1:c.*1603C>A	ENSP00000491240.1:n.*1603C>A
ENST00000639424.1:c.*622C>A	ENSP00000491245.1:n.*622C>A
ENST00000639683.1:c.1356C>A	ENSP00000492581.1:p.Tyr452Ter
ENST00000639975.1:c.1332C>A	ENSP00000492096.1:p.Tyr444Ter
ENST00000640500.1:n.696C>A
ENST00000640739.1:n.6369C>A
ENST00000640910.1:c.860C>A
ENST00000640985.1:c.1335C>A	ENSP00000492293.1:p.Tyr445Ter
ENST00000641017.1:c.1491C>A	ENSP00000493461.1:p.Tyr497Ter
ENST00000356592.7:c.1422C>A	ENSP00000349000.3:p.Tyr474Ter
ENST00000361925.8:c.1398C>A	ENSP00000354651.4:p.Tyr466Ter
ENST00000414552.6:c.1542C>A	ENSP00000410732.2:p.Tyr514Ter
ENST00000522990.5:c.*1000C>A	ENSP00000430732.1:n.*1000C>A
ENST00000523372.1:c.1519C>A	ENSP00000430124.1:n.1519C>A
NM_000816.3:c.1398C>A	NP_000807.2:p.Tyr466Ter
NM_198903.2:c.1542C>A	NP_944493.2:p.Tyr514Ter
NM_198904.2:c.1422C>A	NP_944494.1:p.Tyr474Ter
NM_001375339.1:c.1413C>A	NP_001362268.1:p.Tyr471Ter
NM_001375340.1:c.*256C>A	NP_001362269.1:n.*256C>A
NM_001375341.1:c.1419C>A	NP_001362270.1:p.Tyr473Ter
NM_001375342.1:c.1395C>A	NP_001362271.1:p.Tyr465Ter
NM_001375343.1:c.1518C>A	NP_001362272.1:p.Tyr506Ter
NM_001375344.1:c.1461C>A	NP_001362273.1:p.Tyr487Ter
NM_001375345.1:c.1332C>A	NP_001362274.1:p.Tyr444Ter
NM_001375346.1:c.1356C>A	NP_001362275.1:p.Tyr452Ter
NM_001375347.1:c.1335C>A	NP_001362276.1:p.Tyr445Ter
NM_001375348.1:c.978C>A	NP_001362277.1:p.Tyr326Ter
NM_001375349.1:c.1113C>A	NP_001362278.1:p.Tyr371Ter
NM_001375350.1:c.1002C>A	NP_001362279.1:p.Tyr334Ter
NM_198904.3:c.1422C>A	NP_944494.1:p.Tyr474Ter
NM_198904.4:c.1422C>A MANE Select	NP_944494.1:p.Tyr474Ter