Canonical Allele Identifier: CA2634487250

Gene: GAN

Linked Data

• gnomAD v4: 16-81315012-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81315012_81315013insC , CM000678.2:g.81315012_81315013insC	GRCh38
NC_000016.9:g.81348617_81348618insC , CM000678.1:g.81348617_81348618insC	GRCh37
NC_000016.8:g.79906118_79906119insC	NCBI36
NG_009007.1:g.5047_5048insC , LRG_242:g.5047_5048insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.-102_-101insC	ENSP00000498114.1:n.-102_-101insC
ENST00000648994.2:c.-102_-101insC MANE Select	ENSP00000497351.1:n.-102_-101insC
ENST00000674788.1:n.24_25insC
ENST00000568107.2:c.-102_-101insC	ENSP00000476795.1:n.-102_-101insC
NM_022041.3:c.-102_-101insC , LRG_242t1:c.-102_-101insC	NP_071324.1:n.-102_-101insC
XM_017023734.1:c.-626_-625insC	XP_016879223.1:n.-626_-625insC
NM_001377486.1:c.-626_-625insC	NP_001364415.1:n.-626_-625insC
NM_022041.4:c.-102_-101insC MANE Select	NP_071324.1:n.-102_-101insC