Canonical Allele Identifier: CA365218003

Gene: FIG4

Linked Data

• MyVariant Identifiers: chr6:g.110113869T>G (hg19) ; chr6:g.109792666T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109792666T>G , CM000668.2:g.109792666T>G	GRCh38
NC_000006.11:g.110113869T>G , CM000668.1:g.110113869T>G	GRCh37
NC_000006.10:g.110220562T>G	NCBI36
NG_007977.1:g.106446T>G , LRG_241:g.106446T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000230124.8:c.2459+2T>G MANE Select	ENSP00000230124.4:n.2459+2T>G
ENST00000415980.2:c.965+2T>G	ENSP00000405660.2:n.965+2T>G
ENST00000419951.2:n.807+2T>G
ENST00000674532.1:n.5655+2T>G
ENST00000674557.1:c.*1752+2T>G	ENSP00000501608.1:n.*1752+2T>G
ENST00000674569.1:c.*1578+2T>G	ENSP00000502769.1:n.*1578+2T>G
ENST00000674571.1:c.*1578+2T>G	ENSP00000501633.1:n.*1578+2T>G
ENST00000674575.1:c.*1578+2T>G	ENSP00000502276.1:n.*1578+2T>G
ENST00000674641.1:c.2114+2T>G	ENSP00000501609.1:n.2114+2T>G
ENST00000674649.1:c.*2152+2T>G	ENSP00000501669.1:n.*2152+2T>G
ENST00000674657.1:c.*1891+2T>G	ENSP00000502314.1:n.*1891+2T>G
ENST00000674744.1:c.2453+2T>G	ENSP00000501661.1:n.2453+2T>G
ENST00000674778.1:c.*1677+2T>G	ENSP00000502742.1:n.*1677+2T>G
ENST00000674783.1:c.*1374+2T>G	ENSP00000502755.1:n.*1374+2T>G
ENST00000674884.1:c.2477+2T>G	ENSP00000502668.1:n.2477+2T>G
ENST00000674930.1:c.*1584+2T>G	ENSP00000502657.1:n.*1584+2T>G
ENST00000674933.1:c.2228+2T>G	ENSP00000502376.1:n.2228+2T>G
ENST00000674956.1:c.*1673+2T>G	ENSP00000501904.1:n.*1673+2T>G
ENST00000675004.1:c.*2411+2T>G	ENSP00000501868.1:n.*2411+2T>G
ENST00000675009.1:c.*1843+2T>G	ENSP00000502098.1:n.*1843+2T>G
ENST00000675096.1:c.2252+2T>G	ENSP00000502116.1:n.2252+2T>G
ENST00000675122.1:c.*566+2T>G	ENSP00000501810.1:n.*566+2T>G
ENST00000675153.1:c.*1176+2T>G	ENSP00000501682.1:n.*1176+2T>G
ENST00000675254.1:n.3918+2T>G
ENST00000675272.1:n.6757+2T>G
ENST00000675284.1:c.2459+2T>G	ENSP00000502758.1:n.2459+2T>G
ENST00000675301.1:n.1116+2T>G
ENST00000675311.1:c.*1661+2T>G	ENSP00000501961.1:n.*1661+2T>G
ENST00000675426.1:c.*1527+2T>G	ENSP00000501819.1:n.*1527+2T>G
ENST00000675523.1:c.2228+2T>G	ENSP00000502384.1:n.2228+2T>G
ENST00000675552.1:c.*4722+2T>G	ENSP00000502197.1:n.*4722+2T>G
ENST00000675726.1:c.2459+2T>G	ENSP00000502452.1:n.2459+2T>G
ENST00000675772.1:c.2459+2T>G	ENSP00000501678.1:n.2459+2T>G
ENST00000675831.1:c.2066+2T>G	ENSP00000502382.1:n.2066+2T>G
ENST00000675849.1:n.2081+2T>G
ENST00000675879.1:c.1304+2T>G
ENST00000675954.1:n.3792+2T>G
ENST00000675991.1:c.*4286+2T>G	ENSP00000502162.1:n.*4286+2T>G
ENST00000675994.1:c.*1598+2T>G	ENSP00000502419.1:n.*1598+2T>G
ENST00000676021.1:c.*1037+2T>G	ENSP00000502746.1:n.*1037+2T>G
ENST00000676037.1:c.*386+2T>G	ENSP00000502181.1:n.*386+2T>G
ENST00000676136.1:n.5106+2T>G
ENST00000676246.1:n.349+2T>G
ENST00000676442.1:c.2330+2T>G	ENSP00000502595.1:n.2330+2T>G
ENST00000230124.7:c.2459+2T>G	ENSP00000230124.3:n.2459+2T>G
NM_014845.5:c.2459+2T>G , LRG_241t1:c.2459+2T>G	NP_055660.1:n.2459+2T>G
XM_011536281.1:c.2396+2T>G	XP_011534583.1:n.2396+2T>G
XM_011536281.3:c.2396+2T>G	XP_011534583.1:n.2396+2T>G
XM_017011592.1:c.1910+2T>G	XP_016867081.1:n.1910+2T>G
XM_017011593.2:c.1529+2T>G	XP_016867082.1:n.1529+2T>G
NM_014845.6:c.2459+2T>G MANE Select	NP_055660.1:n.2459+2T>G