Canonical Allele Identifier: CA93633755
Gene: ANAPC4 HGNC NCBI

Linked Data

dbSNP Id: rs16877106
gnomAD v2: 4-25403266-C-T
gnomAD v3: 4-25401644-C-T
gnomAD v4: 4-25401644-C-T
MyVariant Identifiers: chr4:g.25403266C>T (hg19) chr4:g.25401644C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25401644C>T , CM000666.2:g.25401644C>T GRCh38
NC_000004.11:g.25403266C>T , CM000666.1:g.25403266C>T GRCh37
NC_000004.10:g.25012364C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000315368.8:c.1215-1327C>T MANE Select ENSP00000318775.3:n.1215-1327C>T
ENST00000315368.7:c.1215-1327C>T ENSP00000318775.3:n.1215-1327C>T
ENST00000503805.5:n.302-1327C>T
ENST00000505842.5:n.99-1327C>T
ENST00000510092.5:c.1215-1327C>T ENSP00000426654.1:n.1215-1327C>T
NM_001286756.1:c.1215-1327C>T NP_001273685.1:n.1215-1327C>T
NM_013367.2:c.1215-1327C>T NP_037499.2:n.1215-1327C>T
XM_005248159.2:c.111-1327C>T XP_005248216.1:n.111-1327C>T
XM_011513838.1:c.879-1327C>T XP_011512140.1:n.879-1327C>T
XM_011513839.1:c.1215-1327C>T XP_011512141.1:n.1215-1327C>T
XM_017008138.2:c.111-1327C>T XP_016863627.1:n.111-1327C>T
XM_024454027.1:c.111-1327C>T XP_024309795.1:n.111-1327C>T
XR_001741213.1:n.1265-1327C>T
XR_002959726.1:n.1265-1327C>T
NM_001286756.2:c.1215-1327C>T NP_001273685.1:n.1215-1327C>T
NM_013367.3:c.1215-1327C>T MANE Select NP_037499.2:n.1215-1327C>T
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