Canonical Allele Identifier: CA396873151

Gene: GAN

Linked Data

• gnomAD v4: 16-81357832-A-T
• MyVariant Identifiers: chr16:g.81391437A>T (hg19) ; chr16:g.81357832A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81357832A>T , CM000678.2:g.81357832A>T	GRCh38
NC_000016.9:g.81391437A>T , CM000678.1:g.81391437A>T	GRCh37
NC_000016.8:g.79948938A>T	NCBI36
NG_009007.1:g.47867A>T , LRG_242:g.47867A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.*582A>T	ENSP00000498114.1:n.*582A>T
ENST00000648994.2:c.874A>T MANE Select	ENSP00000497351.1:p.Met292Leu
ENST00000650388.1:c.408A>T	ENSP00000498081.1:n.408A>T
ENST00000568107.2:c.874A>T	ENSP00000476795.1:p.Met292Leu
NM_022041.3:c.874A>T , LRG_242t1:c.874A>T	NP_071324.1:p.Met292Leu
XM_017023734.1:c.235A>T	XP_016879223.1:p.Met79Leu
NM_001377486.1:c.235A>T	NP_001364415.1:p.Met79Leu
NM_022041.4:c.874A>T MANE Select	NP_071324.1:p.Met292Leu