Canonical Allele Identifier: CA2634487615

Gene: GAN

Linked Data

• gnomAD v4: 16-81315399-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81315399_81315400insA , CM000678.2:g.81315399_81315400insA	GRCh38
NC_000016.9:g.81349004_81349005insA , CM000678.1:g.81349004_81349005insA	GRCh37
NC_000016.8:g.79906505_79906506insA	NCBI36
NG_009007.1:g.5434_5435insA , LRG_242:g.5434_5435insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.167+119_167+120insA	ENSP00000498114.1:n.167+119_167+120insA
ENST00000648994.2:c.167+119_167+120insA MANE Select	ENSP00000497351.1:n.167+119_167+120insA
ENST00000650388.1:c.167+119_167+120insA	ENSP00000498081.1:n.167+119_167+120insA
ENST00000674788.1:n.292+119_292+120insA
ENST00000568107.2:c.167+119_167+120insA	ENSP00000476795.1:n.167+119_167+120insA
NM_022041.3:c.167+119_167+120insA , LRG_242t1:c.167+119_167+120insA	NP_071324.1:n.167+119_167+120insA
XM_017023734.1:c.-358+119_-358+120insA	XP_016879223.1:n.-358+119_-358+120insA
NM_001377486.1:c.-358+119_-358+120insA	NP_001364415.1:n.-358+119_-358+120insA
NM_022041.4:c.167+119_167+120insA MANE Select	NP_071324.1:n.167+119_167+120insA