Canonical Allele Identifier: CA2497045042
Gene: GRAMD1C HGNC NCBI

Linked Data

dbSNP Id: rs1934606201

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.113866892_113866896del , CM000665.2:g.113866892_113866896del GRCh38
NC_000003.11:g.113585739_113585743del , CM000665.1:g.113585739_113585743del GRCh37
NC_000003.10:g.115068429_115068433del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000358160.9:c.175-2615_175-2611del MANE Select ENSP00000350881.4:n.175-2615_175-2611del
ENST00000358160.8:c.175-2615_175-2611del ENSP00000350881.4:n.175-2615_175-2611del
ENST00000463760.2:n.38-2615_38-2611del
ENST00000472384.5:c.175-2615_175-2611del ENSP00000417936.1:n.175-2615_175-2611del
ENST00000479212.5:n.246-2615_246-2611del
ENST00000484714.2:c.175-2615_175-2611del ENSP00000418501.2:n.175-2615_175-2611del
ENST00000486457.5:n.211-2615_211-2611del
ENST00000498183.5:n.267-2615_267-2611del
NM_017577.4:c.175-2615_175-2611del NP_060047.3:n.175-2615_175-2611del
XM_005247546.1:c.175-2615_175-2611del XP_005247603.1:n.175-2615_175-2611del
XM_005247547.1:c.175-2615_175-2611del XP_005247604.1:n.175-2615_175-2611del
XM_011512930.1:c.145-2615_145-2611del XP_011511232.1:n.145-2615_145-2611del
XM_011512932.1:c.175-2615_175-2611del XP_011511234.1:n.175-2615_175-2611del
XM_005247546.2:c.175-2615_175-2611del XP_005247603.1:n.175-2615_175-2611del
XM_005247547.2:c.175-2615_175-2611del XP_005247604.1:n.175-2615_175-2611del
XM_017006646.1:c.175-2615_175-2611del XP_016862135.1:n.175-2615_175-2611del
XM_017006647.1:c.-727-2615_-727-2611del XP_016862136.1:n.-727-2615_-727-2611del
NM_017577.5:c.175-2615_175-2611del MANE Select NP_060047.3:n.175-2615_175-2611del