Canonical Allele Identifier: CA979655805

Gene: GAN

Linked Data

• gnomAD v3: 16-81354235-CTCTTGG-C
• gnomAD v4: 16-81354235-CTCTTGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81354236_81354241del , CM000678.2:g.81354236_81354241del	GRCh38
NC_000016.9:g.81387841_81387846del , CM000678.1:g.81387841_81387846del	GRCh37
NC_000016.8:g.79945342_79945347del	NCBI36
NG_009007.1:g.44271_44276del , LRG_242:g.44271_44276del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.168-169_168-164del	ENSP00000498114.1:n.168-169_168-164del
ENST00000648994.2:c.283-169_283-164del MANE Select	ENSP00000497351.1:n.283-169_283-164del
ENST00000650388.1:c.168-2549_168-2544del	ENSP00000498081.1:n.168-2549_168-2544del
ENST00000674788.1:n.408-169_408-164del
ENST00000568107.2:c.283-169_283-164del	ENSP00000476795.1:n.283-169_283-164del
NM_022041.3:c.283-169_283-164del , LRG_242t1:c.283-169_283-164del	NP_071324.1:n.283-169_283-164del
XM_017023734.1:c.-357-169_-357-164del	XP_016879223.1:n.-357-169_-357-164del
NM_001377486.1:c.-357-169_-357-164del	NP_001364415.1:n.-357-169_-357-164del
NM_022041.4:c.283-169_283-164del MANE Select	NP_071324.1:n.283-169_283-164del