Canonical Allele Identifier: CA2237033689

Gene: GAN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81354793_81354794delinsTA , CM000678.2:g.81354793_81354794delinsTA	GRCh38
NC_000016.9:g.81388398_81388399delinsTA , CM000678.1:g.81388398_81388399delinsTA	GRCh37
NC_000016.8:g.79945899_79945900delinsTA	NCBI36
NG_009007.1:g.44828_44829delinsTA , LRG_242:g.44828_44829delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.*341+38_*341+39delinsTA	ENSP00000498114.1:n.*341+38_*341+39delinsTA
ENST00000648994.2:c.633+38_633+39delinsTA MANE Select	ENSP00000497351.1:n.633+38_633+39delinsTA
ENST00000650388.1:c.168-1992_168-1991delinsTA	ENSP00000498081.1:n.168-1992_168-1991delinsTA
ENST00000674788.1:n.796_797delinsTA
ENST00000568107.2:c.633+38_633+39delinsTA	ENSP00000476795.1:n.633+38_633+39delinsTA
NM_022041.3:c.633+38_633+39delinsTA , LRG_242t1:c.633+38_633+39delinsTA	NP_071324.1:n.633+38_633+39delinsTA
XM_017023734.1:c.-7+38_-7+39delinsTA	XP_016879223.1:n.-7+38_-7+39delinsTA
NM_001377486.1:c.-7+38_-7+39delinsTA	NP_001364415.1:n.-7+38_-7+39delinsTA
NM_022041.4:c.633+38_633+39delinsTA MANE Select	NP_071324.1:n.633+38_633+39delinsTA