Canonical Allele Identifier: CA545548410

Gene: GRAMD1C

Linked Data

• gnomAD v2: 3-113585672-A-T
• gnomAD v3: 3-113866825-A-T
• gnomAD v4: 3-113866825-A-T
• MyVariant Identifiers: chr3:g.113585672A>T (hg19) ; chr3:g.113866825A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.113866825A>T , CM000665.2:g.113866825A>T	GRCh38
NC_000003.11:g.113585672A>T , CM000665.1:g.113585672A>T	GRCh37
NC_000003.10:g.115068362A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000358160.9:c.175-2682A>T MANE Select	ENSP00000350881.4:n.175-2682A>T
ENST00000358160.8:c.175-2682A>T	ENSP00000350881.4:n.175-2682A>T
ENST00000463760.2:n.38-2682A>T
ENST00000472384.5:c.175-2682A>T	ENSP00000417936.1:n.175-2682A>T
ENST00000479212.5:n.246-2682A>T
ENST00000484714.2:c.175-2682A>T	ENSP00000418501.2:n.175-2682A>T
ENST00000486457.5:n.211-2682A>T
ENST00000498183.5:n.267-2682A>T
NM_017577.4:c.175-2682A>T	NP_060047.3:n.175-2682A>T
XM_005247546.1:c.175-2682A>T	XP_005247603.1:n.175-2682A>T
XM_005247547.1:c.175-2682A>T	XP_005247604.1:n.175-2682A>T
XM_011512930.1:c.145-2682A>T	XP_011511232.1:n.145-2682A>T
XM_011512932.1:c.175-2682A>T	XP_011511234.1:n.175-2682A>T
XM_005247546.2:c.175-2682A>T	XP_005247603.1:n.175-2682A>T
XM_005247547.2:c.175-2682A>T	XP_005247604.1:n.175-2682A>T
XM_017006646.1:c.175-2682A>T	XP_016862135.1:n.175-2682A>T
XM_017006647.1:c.-727-2682A>T	XP_016862136.1:n.-727-2682A>T
NM_017577.5:c.175-2682A>T MANE Select	NP_060047.3:n.175-2682A>T