Canonical Allele Identifier: CA1038267553
Gene: CYTIP HGNC NCBI

Linked Data

dbSNP Id: rs1685524550
gnomAD v3: 2-157421703-C-CAATGA
gnomAD v4: 2-157421703-C-CAATGA
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.157421705_157421709dup , CM000664.2:g.157421705_157421709dup GRCh38
NC_000002.11:g.158278217_158278221dup , CM000664.1:g.158278217_158278221dup GRCh37
NC_000002.10:g.157986463_157986467dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264192.8:c.547-3119_547-3115dup MANE Select ENSP00000264192.3:n.547-3119_547-3115dup
ENST00000264192.7:c.547-3119_547-3115dup ENSP00000264192.3:n.547-3119_547-3115dup
ENST00000418920.5:c.229-3119_229-3115dup ENSP00000394308.1:n.229-3119_229-3115dup
ENST00000457793.6:c.*442-3119_*442-3115dup ENSP00000407205.2:n.*442-3119_*442-3115dup
NM_004288.4:c.547-3119_547-3115dup NP_004279.3:n.547-3119_547-3115dup
XM_017005386.2:c.229-3119_229-3115dup XP_016860875.1:n.229-3119_229-3115dup
NM_004288.5:c.547-3119_547-3115dup MANE Select NP_004279.3:n.547-3119_547-3115dup
Search 100 bp 5'
Search 100 bp 3'