Canonical Allele Identifier: CA13196185

Gene: ZMIZ1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79307723C>G , CM000672.2:g.79307723C>G	GRCh38
NC_000010.10:g.81067480C>G , CM000672.1:g.81067480C>G	GRCh37
NC_000010.9:g.80737486C>G	NCBI36
NG_028289.1:g.243689C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334512.10:c.2835+152C>G MANE Select	ENSP00000334474.5:n.2835+152C>G
ENST00000334512.9:c.2835+152C>G	ENSP00000334474.5:n.2835+152C>G
ENST00000446377.3:c.2538+152C>G	ENSP00000401558.3:n.2538+152C>G
ENST00000611351.1:c.459-6331C>G	ENSP00000481736.1:n.459-6331C>G
NM_020338.3:c.2835+152C>G	NP_065071.1:n.2835+152C>G
XM_005269987.3:c.2853+152C>G	XP_005270044.1:n.2853+152C>G
XM_005269988.2:c.2853+152C>G	XP_005270045.1:n.2853+152C>G
XM_006717923.2:c.2853+152C>G	XP_006717986.1:n.2853+152C>G
XM_006717924.2:c.2853+152C>G	XP_006717987.1:n.2853+152C>G
XM_006717925.2:c.2853+152C>G	XP_006717988.1:n.2853+152C>G
XM_011539978.1:c.2481+152C>G	XP_011538280.1:n.2481+152C>G
XM_011539979.1:c.2481+152C>G	XP_011538281.1:n.2481+152C>G
XM_011539980.1:c.2463+152C>G	XP_011538282.1:n.2463+152C>G
XM_005269987.5:c.2853+152C>G	XP_005270044.1:n.2853+152C>G
XM_005269988.3:c.2853+152C>G	XP_005270045.1:n.2853+152C>G
XM_006717923.3:c.2853+152C>G	XP_006717986.1:n.2853+152C>G
XM_006717924.3:c.2853+152C>G	XP_006717987.1:n.2853+152C>G
XM_006717925.3:c.2853+152C>G	XP_006717988.1:n.2853+152C>G
XM_011539978.2:c.2481+152C>G	XP_011538280.1:n.2481+152C>G
XM_011539980.3:c.2463+152C>G	XP_011538282.1:n.2463+152C>G
XM_017016440.2:c.2700+152C>G	XP_016871929.1:n.2700+152C>G
XM_017016441.1:c.2481+152C>G	XP_016871930.1:n.2481+152C>G
XM_017016442.1:c.2463+152C>G	XP_016871931.1:n.2463+152C>G
XM_017016443.1:c.2481+152C>G	XP_016871932.1:n.2481+152C>G
NM_020338.4:c.2835+152C>G MANE Select	NP_065071.1:n.2835+152C>G