Canonical Allele Identifier: CA2634487936

Gene: GAN

Linked Data

• gnomAD v4: 16-81354825-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81354825_81354826insC , CM000678.2:g.81354825_81354826insC	GRCh38
NC_000016.9:g.81388430_81388431insC , CM000678.1:g.81388430_81388431insC	GRCh37
NC_000016.8:g.79945931_79945932insC	NCBI36
NG_009007.1:g.44860_44861insC , LRG_242:g.44860_44861insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.*341+70_*341+71insC	ENSP00000498114.1:n.*341+70_*341+71insC
ENST00000648994.2:c.633+70_633+71insC MANE Select	ENSP00000497351.1:n.633+70_633+71insC
ENST00000650388.1:c.168-1960_168-1959insC	ENSP00000498081.1:n.168-1960_168-1959insC
ENST00000674788.1:n.828_829insC
ENST00000568107.2:c.633+70_633+71insC	ENSP00000476795.1:n.633+70_633+71insC
NM_022041.3:c.633+70_633+71insC , LRG_242t1:c.633+70_633+71insC	NP_071324.1:n.633+70_633+71insC
XM_017023734.1:c.-7+70_-7+71insC	XP_016879223.1:n.-7+70_-7+71insC
NM_001377486.1:c.-7+70_-7+71insC	NP_001364415.1:n.-7+70_-7+71insC
NM_022041.4:c.633+70_633+71insC MANE Select	NP_071324.1:n.633+70_633+71insC