Canonical Allele Identifier: CA163270593

Gene: ZAN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100747483G>C , CM000669.2:g.100747483G>C	GRCh38
NC_000007.13:g.100345106G>C , CM000669.1:g.100345106G>C	GRCh37
NC_000007.12:g.100183042G>C	NCBI36
NG_029544.2:g.18858G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613979.5:c.932-67G>C MANE Select	ENSP00000480750.1:n.932-67G>C
ENST00000538115.5:c.932-67G>C	ENSP00000445091.2:n.932-67G>C
ENST00000542585.5:c.932-67G>C	ENSP00000444427.2:n.932-67G>C
ENST00000546213.5:c.932-67G>C	ENSP00000441117.2:n.932-67G>C
ENST00000546292.2:c.932-67G>C	ENSP00000445943.2:n.932-67G>C
ENST00000613979.4:c.932-67G>C	ENSP00000480750.1:n.932-67G>C
ENST00000618565.4:c.932-67G>C	ENSP00000478371.1:n.932-67G>C
ENST00000620596.4:c.932-67G>C	ENSP00000481742.1:n.932-67G>C
ENST00000620868.4:n.1097-67G>C
NM_003386.2:c.932-67G>C	NP_003377.2:n.932-67G>C
NM_173059.2:c.932-67G>C	NP_775082.2:n.932-67G>C
NR_111917.1:n.1097-67G>C
NR_111918.1:n.1097-67G>C
NR_111919.1:n.1097-67G>C
XM_011516555.1:c.932-67G>C	XP_011514857.1:n.932-67G>C
XM_011516555.2:c.932-67G>C	XP_011514857.1:n.932-67G>C
NM_003386.3:c.932-67G>C MANE Select	NP_003377.2:n.932-67G>C
NM_173059.3:c.932-67G>C	NP_775082.2:n.932-67G>C
NR_111917.2:n.1128-67G>C
NR_111918.2:n.1128-67G>C
NR_111919.2:n.1128-67G>C