Canonical Allele Identifier: CA545548418

Gene: GRAMD1C

Linked Data

• gnomAD v2: 3-113585682-C-CTTTTT
• MyVariant Identifiers: chr3:g.113585683_113585684insTTTTT (hg19) ; chr3:g.113866836_113866837insTTTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.113866842_113866846dup , CM000665.2:g.113866842_113866846dup	GRCh38
NC_000003.11:g.113585689_113585693dup , CM000665.1:g.113585689_113585693dup	GRCh37
NC_000003.10:g.115068379_115068383dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000358160.9:c.175-2665_175-2661dup MANE Select	ENSP00000350881.4:n.175-2665_175-2661dup
ENST00000358160.8:c.175-2665_175-2661dup	ENSP00000350881.4:n.175-2665_175-2661dup
ENST00000463760.2:n.38-2665_38-2661dup
ENST00000472384.5:c.175-2665_175-2661dup	ENSP00000417936.1:n.175-2665_175-2661dup
ENST00000479212.5:n.246-2665_246-2661dup
ENST00000484714.2:c.175-2665_175-2661dup	ENSP00000418501.2:n.175-2665_175-2661dup
ENST00000486457.5:n.211-2665_211-2661dup
ENST00000498183.5:n.267-2665_267-2661dup
NM_017577.4:c.175-2665_175-2661dup	NP_060047.3:n.175-2665_175-2661dup
XM_005247546.1:c.175-2665_175-2661dup	XP_005247603.1:n.175-2665_175-2661dup
XM_005247547.1:c.175-2665_175-2661dup	XP_005247604.1:n.175-2665_175-2661dup
XM_011512930.1:c.145-2665_145-2661dup	XP_011511232.1:n.145-2665_145-2661dup
XM_011512932.1:c.175-2665_175-2661dup	XP_011511234.1:n.175-2665_175-2661dup
XM_005247546.2:c.175-2665_175-2661dup	XP_005247603.1:n.175-2665_175-2661dup
XM_005247547.2:c.175-2665_175-2661dup	XP_005247604.1:n.175-2665_175-2661dup
XM_017006646.1:c.175-2665_175-2661dup	XP_016862135.1:n.175-2665_175-2661dup
XM_017006647.1:c.-727-2665_-727-2661dup	XP_016862136.1:n.-727-2665_-727-2661dup
NM_017577.5:c.175-2665_175-2661dup MANE Select	NP_060047.3:n.175-2665_175-2661dup