Canonical Allele Identifier: CA2237006792

Gene: GAN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81365546_81365551delinsTGTTTA , CM000678.2:g.81365546_81365551delinsTGTTTA	GRCh38
NC_000016.9:g.81399151_81399156delinsTGTTTA , CM000678.1:g.81399151_81399156delinsTGTTTA	GRCh37
NC_000016.8:g.79956652_79956657delinsTGTTTA	NCBI36
NG_009007.1:g.55581_55586delinsTGTTTA , LRG_242:g.55581_55586delinsTGTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.*1210+68_*1210+73delinsTGTTTA	ENSP00000498114.1:n.*1210+68_*1210+73delinsTGTTTA
ENST00000648994.2:c.1502+68_1502+73delinsTGTTTA MANE Select	ENSP00000497351.1:n.1502+68_1502+73delinsTGTTTA
ENST00000650388.1:c.1036+68_1036+73delinsTGTTTA	ENSP00000498081.1:n.1036+68_1036+73delinsTGTTTA
ENST00000567335.1:n.60+68_60+73delinsTGTTTA
ENST00000568107.2:c.1502+68_1502+73delinsTGTTTA	ENSP00000476795.1:n.1502+68_1502+73delinsTGTTTA
NM_022041.3:c.1502+68_1502+73delinsTGTTTA , LRG_242t1:c.1502+68_1502+73delinsTGTTTA	NP_071324.1:n.1502+68_1502+73delinsTGTTTA
XM_017023734.1:c.863+68_863+73delinsTGTTTA	XP_016879223.1:n.863+68_863+73delinsTGTTTA
NM_001377486.1:c.863+68_863+73delinsTGTTTA	NP_001364415.1:n.863+68_863+73delinsTGTTTA
NM_022041.4:c.1502+68_1502+73delinsTGTTTA MANE Select	NP_071324.1:n.1502+68_1502+73delinsTGTTTA