Canonical Allele Identifier: CA2237043098

Gene: GAN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81358108_81358111delinsCTTA , CM000678.2:g.81358108_81358111delinsCTTA	GRCh38
NC_000016.9:g.81391713_81391716delinsCTTA , CM000678.1:g.81391713_81391716delinsCTTA	GRCh37
NC_000016.8:g.79949214_79949217delinsCTTA	NCBI36
NG_009007.1:g.48143_48146delinsCTTA , LRG_242:g.48143_48146delinsCTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.*681+177_*681+180delinsCTTA	ENSP00000498114.1:n.*681+177_*681+180delinsCTTA
ENST00000648994.2:c.973+177_973+180delinsCTTA MANE Select	ENSP00000497351.1:n.973+177_973+180delinsCTTA
ENST00000650388.1:c.507+177_507+180delinsCTTA	ENSP00000498081.1:n.507+177_507+180delinsCTTA
ENST00000568107.2:c.973+177_973+180delinsCTTA	ENSP00000476795.1:n.973+177_973+180delinsCTTA
NM_022041.3:c.973+177_973+180delinsCTTA , LRG_242t1:c.973+177_973+180delinsCTTA	NP_071324.1:n.973+177_973+180delinsCTTA
XM_017023734.1:c.334+177_334+180delinsCTTA	XP_016879223.1:n.334+177_334+180delinsCTTA
NM_001377486.1:c.334+177_334+180delinsCTTA	NP_001364415.1:n.334+177_334+180delinsCTTA
NM_022041.4:c.973+177_973+180delinsCTTA MANE Select	NP_071324.1:n.973+177_973+180delinsCTTA