Canonical Allele Identifier: CA1300943749
Gene: CYTIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.157421758A= , CM000664.2:g.157421758A= GRCh38
NC_000002.11:g.158278270A= , CM000664.1:g.158278270A= GRCh37
NC_000002.10:g.157986516A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264192.8:c.547-3169T= MANE Select ENSP00000264192.3:n.547-3169T=
ENST00000264192.7:c.547-3169T= ENSP00000264192.3:n.547-3169T=
ENST00000418920.5:c.229-3169T= ENSP00000394308.1:n.229-3169T=
ENST00000457793.6:c.*442-3169T= ENSP00000407205.2:n.*442-3169T=
NM_004288.4:c.547-3169T= NP_004279.3:n.547-3169T=
XM_017005386.2:c.229-3169T= XP_016860875.1:n.229-3169T=
NM_004288.5:c.547-3169T= MANE Select NP_004279.3:n.547-3169T=