Canonical Allele Identifier: CA396873489

Gene: GAN

Linked Data

• dbSNP Id: rs1910544567
• MyVariant Identifiers: chr16:g.81391503A>T (hg19) ; chr16:g.81357898A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81357898A>T , CM000678.2:g.81357898A>T	GRCh38
NC_000016.9:g.81391503A>T , CM000678.1:g.81391503A>T	GRCh37
NC_000016.8:g.79949004A>T	NCBI36
NG_009007.1:g.47933A>T , LRG_242:g.47933A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.*648A>T	ENSP00000498114.1:n.*648A>T
ENST00000648994.2:c.940A>T MANE Select	ENSP00000497351.1:p.Met314Leu
ENST00000650388.1:c.474A>T	ENSP00000498081.1:n.474A>T
ENST00000568107.2:c.940A>T	ENSP00000476795.1:p.Met314Leu
NM_022041.3:c.940A>T , LRG_242t1:c.940A>T	NP_071324.1:p.Met314Leu
XM_017023734.1:c.301A>T	XP_016879223.1:p.Met101Leu
NM_001377486.1:c.301A>T	NP_001364415.1:p.Met101Leu
NM_022041.4:c.940A>T MANE Select	NP_071324.1:p.Met314Leu