Canonical Allele Identifier: CA2634487947

Gene: GAN

Linked Data

• gnomAD v4: 16-81354851-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81354852_81354853insAA , CM000678.2:g.81354852_81354853insAA	GRCh38
NC_000016.9:g.81388457_81388458insAA , CM000678.1:g.81388457_81388458insAA	GRCh37
NC_000016.8:g.79945958_79945959insAA	NCBI36
NG_009007.1:g.44887_44888insAA , LRG_242:g.44887_44888insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.*341+97_*341+98insAA	ENSP00000498114.1:n.*341+97_*341+98insAA
ENST00000648994.2:c.633+97_633+98insAA MANE Select	ENSP00000497351.1:n.633+97_633+98insAA
ENST00000650388.1:c.168-1933_168-1932insAA	ENSP00000498081.1:n.168-1933_168-1932insAA
ENST00000674788.1:n.855_856insAA
ENST00000568107.2:c.633+97_633+98insAA	ENSP00000476795.1:n.633+97_633+98insAA
NM_022041.3:c.633+97_633+98insAA , LRG_242t1:c.633+97_633+98insAA	NP_071324.1:n.633+97_633+98insAA
XM_017023734.1:c.-7+97_-7+98insAA	XP_016879223.1:n.-7+97_-7+98insAA
NM_001377486.1:c.-7+97_-7+98insAA	NP_001364415.1:n.-7+97_-7+98insAA
NM_022041.4:c.633+97_633+98insAA MANE Select	NP_071324.1:n.633+97_633+98insAA