Canonical Allele Identifier: CA2634487228

Gene: GAN

Linked Data

• gnomAD v4: 16-81314991-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81314991A>T , CM000678.2:g.81314991A>T	GRCh38
NC_000016.9:g.81348596A>T , CM000678.1:g.81348596A>T	GRCh37
NC_000016.8:g.79906097A>T	NCBI36
NG_009007.1:g.5026A>T , LRG_242:g.5026A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.-123A>T	ENSP00000498114.1:n.-123A>T
ENST00000648994.2:c.-123A>T MANE Select	ENSP00000497351.1:n.-123A>T
ENST00000674788.1:n.3A>T
ENST00000568107.2:c.-123A>T	ENSP00000476795.1:n.-123A>T
NM_022041.3:c.-123A>T , LRG_242t1:c.-123A>T	NP_071324.1:n.-123A>T
XM_017023734.1:c.-647A>T	XP_016879223.1:n.-647A>T
NM_001377486.1:c.-647A>T	NP_001364415.1:n.-647A>T
NM_022041.4:c.-123A>T MANE Select	NP_071324.1:n.-123A>T