Canonical Allele Identifier: CA2634487356

Gene: GAN

Linked Data

• gnomAD v4: 16-81315062-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81315062C>T , CM000678.2:g.81315062C>T	GRCh38
NC_000016.9:g.81348667C>T , CM000678.1:g.81348667C>T	GRCh37
NC_000016.8:g.79906168C>T	NCBI36
NG_009007.1:g.5097C>T , LRG_242:g.5097C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000648349.2:c.-52C>T	ENSP00000498114.1:n.-52C>T
ENST00000648994.2:c.-52C>T MANE Select	ENSP00000497351.1:n.-52C>T
ENST00000674788.1:n.74C>T
ENST00000568107.2:c.-52C>T	ENSP00000476795.1:n.-52C>T
NM_022041.3:c.-52C>T , LRG_242t1:c.-52C>T	NP_071324.1:n.-52C>T
XM_017023734.1:c.-576C>T	XP_016879223.1:n.-576C>T
NM_001377486.1:c.-576C>T	NP_001364415.1:n.-576C>T
NM_022041.4:c.-52C>T MANE Select	NP_071324.1:n.-52C>T