Canonical Allele Identifier: CA2237031727

Gene: GAN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81354256_81354257delinsAT , CM000678.2:g.81354256_81354257delinsAT	GRCh38
NC_000016.9:g.81387861_81387862delinsAT , CM000678.1:g.81387861_81387862delinsAT	GRCh37
NC_000016.8:g.79945362_79945363delinsAT	NCBI36
NG_009007.1:g.44291_44292delinsAT , LRG_242:g.44291_44292delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.168-149_168-148delinsAT	ENSP00000498114.1:n.168-149_168-148delinsAT
ENST00000648994.2:c.283-149_283-148delinsAT MANE Select	ENSP00000497351.1:n.283-149_283-148delinsAT
ENST00000650388.1:c.168-2529_168-2528delinsAT	ENSP00000498081.1:n.168-2529_168-2528delinsAT
ENST00000674788.1:n.408-149_408-148delinsAT
ENST00000568107.2:c.283-149_283-148delinsAT	ENSP00000476795.1:n.283-149_283-148delinsAT
NM_022041.3:c.283-149_283-148delinsAT , LRG_242t1:c.283-149_283-148delinsAT	NP_071324.1:n.283-149_283-148delinsAT
XM_017023734.1:c.-357-149_-357-148delinsAT	XP_016879223.1:n.-357-149_-357-148delinsAT
NM_001377486.1:c.-357-149_-357-148delinsAT	NP_001364415.1:n.-357-149_-357-148delinsAT
NM_022041.4:c.283-149_283-148delinsAT MANE Select	NP_071324.1:n.283-149_283-148delinsAT