Canonical Allele Identifier: CA2497045041

Gene: GRAMD1C

Linked Data

• dbSNP Id: rs1934603540

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.113866837_113866838insCT , CM000665.2:g.113866837_113866838insCT	GRCh38
NC_000003.11:g.113585684_113585685insCT , CM000665.1:g.113585684_113585685insCT	GRCh37
NC_000003.10:g.115068374_115068375insCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358160.9:c.175-2670_175-2669insCT MANE Select	ENSP00000350881.4:n.175-2670_175-2669insCT
ENST00000358160.8:c.175-2670_175-2669insCT	ENSP00000350881.4:n.175-2670_175-2669insCT
ENST00000463760.2:n.38-2670_38-2669insCT
ENST00000472384.5:c.175-2670_175-2669insCT	ENSP00000417936.1:n.175-2670_175-2669insCT
ENST00000479212.5:n.246-2670_246-2669insCT
ENST00000484714.2:c.175-2670_175-2669insCT	ENSP00000418501.2:n.175-2670_175-2669insCT
ENST00000486457.5:n.211-2670_211-2669insCT
ENST00000498183.5:n.267-2670_267-2669insCT
NM_017577.4:c.175-2670_175-2669insCT	NP_060047.3:n.175-2670_175-2669insCT
XM_005247546.1:c.175-2670_175-2669insCT	XP_005247603.1:n.175-2670_175-2669insCT
XM_005247547.1:c.175-2670_175-2669insCT	XP_005247604.1:n.175-2670_175-2669insCT
XM_011512930.1:c.145-2670_145-2669insCT	XP_011511232.1:n.145-2670_145-2669insCT
XM_011512932.1:c.175-2670_175-2669insCT	XP_011511234.1:n.175-2670_175-2669insCT
XM_005247546.2:c.175-2670_175-2669insCT	XP_005247603.1:n.175-2670_175-2669insCT
XM_005247547.2:c.175-2670_175-2669insCT	XP_005247604.1:n.175-2670_175-2669insCT
XM_017006646.1:c.175-2670_175-2669insCT	XP_016862135.1:n.175-2670_175-2669insCT
XM_017006647.1:c.-727-2670_-727-2669insCT	XP_016862136.1:n.-727-2670_-727-2669insCT
NM_017577.5:c.175-2670_175-2669insCT MANE Select	NP_060047.3:n.175-2670_175-2669insCT