Canonical Allele Identifier: CA396854812

Gene: GAN

Linked Data

• MyVariant Identifiers: chr16:g.81348822T>A (hg19) ; chr16:g.81315217T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81315217T>A , CM000678.2:g.81315217T>A	GRCh38
NC_000016.9:g.81348822T>A , CM000678.1:g.81348822T>A	GRCh37
NC_000016.8:g.79906323T>A	NCBI36
NG_009007.1:g.5252T>A , LRG_242:g.5252T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.104T>A	ENSP00000498114.1:p.Val35Asp
ENST00000648994.2:c.104T>A MANE Select	ENSP00000497351.1:p.Val35Asp
ENST00000650388.1:c.104T>A	ENSP00000498081.1:p.Val35Asp
ENST00000674788.1:n.229T>A
ENST00000568107.2:c.104T>A	ENSP00000476795.1:p.Val35Asp
NM_022041.3:c.104T>A , LRG_242t1:c.104T>A	NP_071324.1:p.Val35Asp
XM_017023734.1:c.-421T>A	XP_016879223.1:n.-421T>A
NM_001377486.1:c.-421T>A	NP_001364415.1:n.-421T>A
NM_022041.4:c.104T>A MANE Select	NP_071324.1:p.Val35Asp