Canonical Allele Identifier: CA591341024

Gene: DIP2C

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.520439C>A , CM000672.2:g.520439C>A	GRCh38
NC_000010.10:g.566379C>A , CM000672.1:g.566379C>A	GRCh37
NC_000010.9:g.556379C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280886.12:c.86-33909G>T MANE Select	ENSP00000280886.6:n.86-33909G>T
ENST00000280886.11:c.86-33909G>T	ENSP00000280886.6:n.86-33909G>T
ENST00000634311.1:c.86-33909G>T	ENSP00000489203.1:n.86-33909G>T
NM_014974.2:c.86-33909G>T	NP_055789.1:n.86-33909G>T
XM_005252426.2:c.86-33909G>T	XP_005252483.1:n.86-33909G>T
XM_005252427.2:c.86-33909G>T	XP_005252484.1:n.86-33909G>T
XM_005252428.3:c.86-33909G>T	XP_005252485.1:n.86-33909G>T
XM_011519432.1:c.-236-33909G>T	XP_011517734.1:n.-236-33909G>T
XM_005252426.3:c.86-33909G>T	XP_005252483.1:n.86-33909G>T
XM_005252427.4:c.86-33909G>T	XP_005252484.1:n.86-33909G>T
XM_005252428.4:c.86-33909G>T	XP_005252485.1:n.86-33909G>T
XM_011519432.2:c.-236-33909G>T	XP_011517734.1:n.-236-33909G>T
NM_014974.3:c.86-33909G>T MANE Select	NP_055789.1:n.86-33909G>T