Canonical Allele Identifier: CA1978634881

Gene: STIP1

Linked Data

• dbSNP Id: rs1946150600

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196396A>C , CM000673.2:g.64196396A>C	GRCh38
NC_000011.9:g.63963868A>C , CM000673.1:g.63963868A>C	GRCh37
NC_000011.8:g.63720444A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.672+583A>C MANE Select	ENSP00000305958.5:n.672+583A>C
ENST00000305218.8:c.672+583A>C	ENSP00000305958.4:n.672+583A>C
ENST00000358794.9:c.813+583A>C	ENSP00000351646.5:n.813+583A>C
ENST00000536973.5:c.361+2066A>C	ENSP00000441036.1:n.361+2066A>C
ENST00000538945.5:c.600+583A>C	ENSP00000445957.1:n.600+583A>C
NM_001282652.1:c.813+583A>C	NP_001269581.1:n.813+583A>C
NM_001282653.1:c.600+583A>C	NP_001269582.1:n.600+583A>C
NM_006819.2:c.672+583A>C	NP_006810.1:n.672+583A>C
NM_001282653.2:c.600+583A>C	NP_001269582.1:n.600+583A>C
NM_006819.3:c.672+583A>C MANE Select	NP_006810.1:n.672+583A>C
NM_001282652.2:c.813+583A>C	NP_001269581.1:n.813+583A>C