Canonical Allele Identifier: CA2634487934

Gene: GAN

Linked Data

• gnomAD v4: 16-81354824-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81354824_81354825insG , CM000678.2:g.81354824_81354825insG	GRCh38
NC_000016.9:g.81388429_81388430insG , CM000678.1:g.81388429_81388430insG	GRCh37
NC_000016.8:g.79945930_79945931insG	NCBI36
NG_009007.1:g.44859_44860insG , LRG_242:g.44859_44860insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.*341+69_*341+70insG	ENSP00000498114.1:n.*341+69_*341+70insG
ENST00000648994.2:c.633+69_633+70insG MANE Select	ENSP00000497351.1:n.633+69_633+70insG
ENST00000650388.1:c.168-1961_168-1960insG	ENSP00000498081.1:n.168-1961_168-1960insG
ENST00000674788.1:n.827_828insG
ENST00000568107.2:c.633+69_633+70insG	ENSP00000476795.1:n.633+69_633+70insG
NM_022041.3:c.633+69_633+70insG , LRG_242t1:c.633+69_633+70insG	NP_071324.1:n.633+69_633+70insG
XM_017023734.1:c.-7+69_-7+70insG	XP_016879223.1:n.-7+69_-7+70insG
NM_001377486.1:c.-7+69_-7+70insG	NP_001364415.1:n.-7+69_-7+70insG
NM_022041.4:c.633+69_633+70insG MANE Select	NP_071324.1:n.633+69_633+70insG