Canonical Allele Identifier: CA2695224519
Gene: GUCY2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8012608dup , CM000679.2:g.8012608dup GRCh38
NC_000017.10:g.7915926dup , CM000679.1:g.7915926dup GRCh37
NC_000017.9:g.7856651dup NCBI36
NG_009092.1:g.14939dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.2113+2dup MANE Select ENSP00000254854.4:n.2113+2dup
ENST00000254854.4:c.2113+2dup ENSP00000254854.4:n.2113+2dup
NM_000180.3:c.2113+2dup NP_000171.1:n.2113+2dup
XM_011523816.1:c.2113+2dup XP_011522118.1:n.2113+2dup
NM_000180.4:c.2113+2dup MANE Select NP_000171.1:n.2113+2dup