Canonical Allele Identifier: CA1052354339

Gene: GRAMD1C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.113866849_113866850insTTTT , CM000665.2:g.113866849_113866850insTTTT	GRCh38
NC_000003.11:g.113585696_113585697insTTTT , CM000665.1:g.113585696_113585697insTTTT	GRCh37
NC_000003.10:g.115068386_115068387insTTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358160.9:c.175-2658_175-2657insTTTT MANE Select	ENSP00000350881.4:n.175-2658_175-2657insTTTT
ENST00000358160.8:c.175-2658_175-2657insTTTT	ENSP00000350881.4:n.175-2658_175-2657insTTTT
ENST00000463760.2:n.38-2658_38-2657insTTTT
ENST00000472384.5:c.175-2658_175-2657insTTTT	ENSP00000417936.1:n.175-2658_175-2657insTTTT
ENST00000479212.5:n.246-2658_246-2657insTTTT
ENST00000484714.2:c.175-2658_175-2657insTTTT	ENSP00000418501.2:n.175-2658_175-2657insTTTT
ENST00000486457.5:n.211-2658_211-2657insTTTT
ENST00000498183.5:n.267-2658_267-2657insTTTT
NM_017577.4:c.175-2658_175-2657insTTTT	NP_060047.3:n.175-2658_175-2657insTTTT
XM_005247546.1:c.175-2658_175-2657insTTTT	XP_005247603.1:n.175-2658_175-2657insTTTT
XM_005247547.1:c.175-2658_175-2657insTTTT	XP_005247604.1:n.175-2658_175-2657insTTTT
XM_011512930.1:c.145-2658_145-2657insTTTT	XP_011511232.1:n.145-2658_145-2657insTTTT
XM_011512932.1:c.175-2658_175-2657insTTTT	XP_011511234.1:n.175-2658_175-2657insTTTT
XM_005247546.2:c.175-2658_175-2657insTTTT	XP_005247603.1:n.175-2658_175-2657insTTTT
XM_005247547.2:c.175-2658_175-2657insTTTT	XP_005247604.1:n.175-2658_175-2657insTTTT
XM_017006646.1:c.175-2658_175-2657insTTTT	XP_016862135.1:n.175-2658_175-2657insTTTT
XM_017006647.1:c.-727-2658_-727-2657insTTTT	XP_016862136.1:n.-727-2658_-727-2657insTTTT
NM_017577.5:c.175-2658_175-2657insTTTT MANE Select	NP_060047.3:n.175-2658_175-2657insTTTT