Canonical Allele Identifier: CA593963863

Gene: ANK3

Linked Data

• dbSNP Id: rs1164543827
• gnomAD v2: 10-62179848-G-A
• gnomAD v3: 10-60420090-G-A
• gnomAD v4: 10-60420090-G-A
• MyVariant Identifiers: chr10:g.62179848G>A (hg19) ; chr10:g.60420090G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.60420090G>A , CM000672.2:g.60420090G>A	GRCh38
NC_000010.10:g.62179848G>A , CM000672.1:g.62179848G>A	GRCh37
NC_000010.9:g.61849854G>A	NCBI36
NG_029917.1:g.318437C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000503366.6:c.64-140451C>T	ENSP00000425236.1:n.64-140451C>T
ENST00000373827.6:c.97-140451C>T	ENSP00000362933.2:n.97-140451C>T
ENST00000503366.5:c.64-140451C>T	ENSP00000425236.1:n.64-140451C>T
ENST00000622427.4:c.64-140451C>T	ENSP00000483244.1:n.64-140451C>T
NM_001204403.1:c.97-140451C>T	NP_001191332.1:n.97-140451C>T
NM_001204404.1:c.64-140451C>T	NP_001191333.1:n.64-140451C>T
XM_011539700.1:c.103-140451C>T	XP_011538002.1:n.103-140451C>T
XM_011539701.1:c.97-140451C>T	XP_011538003.1:n.97-140451C>T
XM_011539702.1:c.58-140451C>T	XP_011538004.1:n.58-140451C>T
XM_011539704.1:c.15+77894C>T	XP_011538006.1:n.15+77894C>T
XM_017016114.1:c.64-140451C>T	XP_016871603.1:n.64-140451C>T
XM_024447958.1:c.64-140451C>T	XP_024303726.1:n.64-140451C>T
NM_001204403.2:c.97-140451C>T	NP_001191332.1:n.97-140451C>T
NM_001204404.2:c.64-140451C>T	NP_001191333.1:n.64-140451C>T