Canonical Allele Identifier: CA1300943739
Gene: CYTIP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.157421711A= , CM000664.2:g.157421711A= GRCh38
NC_000002.11:g.158278223A= , CM000664.1:g.158278223A= GRCh37
NC_000002.10:g.157986469A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264192.8:c.547-3122T= MANE Select ENSP00000264192.3:n.547-3122T=
ENST00000264192.7:c.547-3122T= ENSP00000264192.3:n.547-3122T=
ENST00000418920.5:c.229-3122T= ENSP00000394308.1:n.229-3122T=
ENST00000457793.6:c.*442-3122T= ENSP00000407205.2:n.*442-3122T=
NM_004288.4:c.547-3122T= NP_004279.3:n.547-3122T=
XM_017005386.2:c.229-3122T= XP_016860875.1:n.229-3122T=
NM_004288.5:c.547-3122T= MANE Select NP_004279.3:n.547-3122T=
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