Canonical Allele Identifier: CA210582176

Gene: ZMIZ1

Linked Data

• dbSNP Id: rs984175538
• gnomAD v2: 10-81015815-T-A
• gnomAD v3: 10-79256058-T-A
• gnomAD v4: 10-79256058-T-A
• MyVariant Identifiers: chr10:g.81015815T>A (hg19) ; chr10:g.79256058T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79256058T>A , CM000672.2:g.79256058T>A	GRCh38
NC_000010.10:g.81015815T>A , CM000672.1:g.81015815T>A	GRCh37
NC_000010.9:g.80685821T>A	NCBI36
NG_028289.1:g.192024T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000334512.10:c.281-21123T>A MANE Select	ENSP00000334474.5:n.281-21123T>A
ENST00000334512.9:c.281-21123T>A	ENSP00000334474.5:n.281-21123T>A
ENST00000472035.5:n.70+12320T>A
ENST00000611351.1:c.281-21123T>A	ENSP00000481736.1:n.281-21123T>A
NM_020338.3:c.281-21123T>A	NP_065071.1:n.281-21123T>A
XM_005269987.3:c.281-21123T>A	XP_005270044.1:n.281-21123T>A
XM_005269988.2:c.281-21123T>A	XP_005270045.1:n.281-21123T>A
XM_006717923.2:c.281-21123T>A	XP_006717986.1:n.281-21123T>A
XM_006717924.2:c.281-21123T>A	XP_006717987.1:n.281-21123T>A
XM_006717925.2:c.281-21123T>A	XP_006717988.1:n.281-21123T>A
XM_011539978.1:c.-93+12320T>A	XP_011538280.1:n.-93+12320T>A
XM_011539979.1:c.-93+13089T>A	XP_011538281.1:n.-93+13089T>A
XM_011539980.1:c.-93+12320T>A	XP_011538282.1:n.-93+12320T>A
XM_005269987.5:c.281-21123T>A	XP_005270044.1:n.281-21123T>A
XM_005269988.3:c.281-21123T>A	XP_005270045.1:n.281-21123T>A
XM_006717923.3:c.281-21123T>A	XP_006717986.1:n.281-21123T>A
XM_006717924.3:c.281-21123T>A	XP_006717987.1:n.281-21123T>A
XM_006717925.3:c.281-21123T>A	XP_006717988.1:n.281-21123T>A
XM_011539978.2:c.-93+12320T>A	XP_011538280.1:n.-93+12320T>A
XM_011539980.3:c.-93+12320T>A	XP_011538282.1:n.-93+12320T>A
XM_017016441.1:c.-93+12988T>A	XP_016871930.1:n.-93+12988T>A
XM_017016442.1:c.-93+13089T>A	XP_016871931.1:n.-93+13089T>A
XM_017016443.1:c.-93+13164T>A	XP_016871932.1:n.-93+13164T>A
NM_020338.4:c.281-21123T>A MANE Select	NP_065071.1:n.281-21123T>A