Canonical Allele Identifier: CA1866927643

Gene: GABBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98442771_98442774delinsCCTT , CM000671.2:g.98442771_98442774delinsCCTT	GRCh38
NC_000009.11:g.101205053_101205056delinsCCTT , CM000671.1:g.101205053_101205056delinsCCTT	GRCh37
NC_000009.10:g.100244874_100244877delinsCCTT	NCBI36
NG_016426.1:g.271424_271427delinsAAGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000259455.4:c.1236+11207_1236+11210delinsAAGG MANE Select	ENSP00000259455.2:n.1236+11207_1236+11210delinsAAGG
ENST00000637410.1:n.1014+11207_1014+11210delinsAAGG
ENST00000259455.3:c.1236+11207_1236+11210delinsAAGG	ENSP00000259455.2:n.1236+11207_1236+11210delinsAAGG
NM_005458.7:c.1236+11207_1236+11210delinsAAGG	NP_005449.5:n.1236+11207_1236+11210delinsAAGG
XM_005252316.3:c.462+11207_462+11210delinsAAGG	XP_005252373.1:n.462+11207_462+11210delinsAAGG
XM_005252316.5:c.462+11207_462+11210delinsAAGG	XP_005252373.1:n.462+11207_462+11210delinsAAGG
XM_017015331.2:c.942+11207_942+11210delinsAAGG	XP_016870820.1:n.942+11207_942+11210delinsAAGG
XM_017015332.2:c.462+11207_462+11210delinsAAGG	XP_016870821.1:n.462+11207_462+11210delinsAAGG
NM_005458.8:c.1236+11207_1236+11210delinsAAGG MANE Select	NP_005449.5:n.1236+11207_1236+11210delinsAAGG