Canonical Allele Identifier: CA2703707099
Gene: GRAMD1C HGNC NCBI

Linked Data

dbSNP Id: rs1934601353

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.113866787A>C , CM000665.2:g.113866787A>C GRCh38
NC_000003.11:g.113585634A>C , CM000665.1:g.113585634A>C GRCh37
NC_000003.10:g.115068324A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000358160.9:c.175-2720A>C MANE Select ENSP00000350881.4:n.175-2720A>C
ENST00000358160.8:c.175-2720A>C ENSP00000350881.4:n.175-2720A>C
ENST00000463760.2:n.38-2720A>C
ENST00000472384.5:c.175-2720A>C ENSP00000417936.1:n.175-2720A>C
ENST00000479212.5:n.246-2720A>C
ENST00000484714.2:c.175-2720A>C ENSP00000418501.2:n.175-2720A>C
ENST00000486457.5:n.211-2720A>C
ENST00000498183.5:n.267-2720A>C
NM_017577.4:c.175-2720A>C NP_060047.3:n.175-2720A>C
XM_005247546.1:c.175-2720A>C XP_005247603.1:n.175-2720A>C
XM_005247547.1:c.175-2720A>C XP_005247604.1:n.175-2720A>C
XM_011512930.1:c.145-2720A>C XP_011511232.1:n.145-2720A>C
XM_011512932.1:c.175-2720A>C XP_011511234.1:n.175-2720A>C
XM_005247546.2:c.175-2720A>C XP_005247603.1:n.175-2720A>C
XM_005247547.2:c.175-2720A>C XP_005247604.1:n.175-2720A>C
XM_017006646.1:c.175-2720A>C XP_016862135.1:n.175-2720A>C
XM_017006647.1:c.-727-2720A>C XP_016862136.1:n.-727-2720A>C
NM_017577.5:c.175-2720A>C MANE Select NP_060047.3:n.175-2720A>C