Canonical Allele Identifier: CA2634487348

Gene: GAN

Linked Data

• gnomAD v4: 16-81315055-AGGGGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81315056_81315060del , CM000678.2:g.81315056_81315060del	GRCh38
NC_000016.9:g.81348661_81348665del , CM000678.1:g.81348661_81348665del	GRCh37
NC_000016.8:g.79906162_79906166del	NCBI36
NG_009007.1:g.5091_5095del , LRG_242:g.5091_5095del

Transcript Alleles

HGVS	Amino-acid change
ENST00000648349.2:c.-58_-54del	ENSP00000498114.1:n.-58_-54del
ENST00000648994.2:c.-58_-54del MANE Select	ENSP00000497351.1:n.-58_-54del
ENST00000674788.1:n.68_72del
ENST00000568107.2:c.-58_-54del	ENSP00000476795.1:n.-58_-54del
NM_022041.3:c.-58_-54del , LRG_242t1:c.-58_-54del	NP_071324.1:n.-58_-54del
XM_017023734.1:c.-582_-578del	XP_016879223.1:n.-582_-578del
NM_001377486.1:c.-582_-578del	NP_001364415.1:n.-582_-578del
NM_022041.4:c.-58_-54del MANE Select	NP_071324.1:n.-58_-54del