Canonical Allele Identifier: CA656816773

Gene: GAN

Linked Data

• COSMIC: COSN1191276

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81354164C>T , CM000678.2:g.81354164C>T	GRCh38
NC_000016.9:g.81387769C>T , CM000678.1:g.81387769C>T	GRCh37
NC_000016.8:g.79945270C>T	NCBI36
NG_009007.1:g.44199C>T , LRG_242:g.44199C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.168-241C>T	ENSP00000498114.1:n.168-241C>T
ENST00000648994.2:c.283-241C>T MANE Select	ENSP00000497351.1:n.283-241C>T
ENST00000650388.1:c.168-2621C>T	ENSP00000498081.1:n.168-2621C>T
ENST00000674788.1:n.408-241C>T
ENST00000568107.2:c.283-241C>T	ENSP00000476795.1:n.283-241C>T
NM_022041.3:c.283-241C>T , LRG_242t1:c.283-241C>T	NP_071324.1:n.283-241C>T
XM_017023734.1:c.-357-241C>T	XP_016879223.1:n.-357-241C>T
NM_001377486.1:c.-357-241C>T	NP_001364415.1:n.-357-241C>T
NM_022041.4:c.283-241C>T MANE Select	NP_071324.1:n.283-241C>T