Canonical Allele Identifier: CA15677641

Gene: STIP1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64191787A>C , CM000673.2:g.64191787A>C	GRCh38
NC_000011.9:g.63959259A>C , CM000673.1:g.63959259A>C	GRCh37
NC_000011.8:g.63715835A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.10-1291A>C MANE Select	ENSP00000305958.5:n.10-1291A>C
ENST00000305218.8:c.10-1291A>C	ENSP00000305958.4:n.10-1291A>C
ENST00000358794.9:c.151-1291A>C	ENSP00000351646.5:n.151-1291A>C
ENST00000536973.5:c.10-1291A>C	ENSP00000441036.1:n.10-1291A>C
ENST00000538945.5:c.10-1291A>C	ENSP00000445957.1:n.10-1291A>C
ENST00000540501.1:n.220-1291A>C
ENST00000540736.1:n.38-1291A>C
ENST00000543847.1:c.10-1291A>C	ENSP00000442704.1:n.10-1291A>C
NM_001282652.1:c.151-1291A>C	NP_001269581.1:n.151-1291A>C
NM_001282653.1:c.10-1291A>C	NP_001269582.1:n.10-1291A>C
NM_006819.2:c.10-1291A>C	NP_006810.1:n.10-1291A>C
NM_001282653.2:c.10-1291A>C	NP_001269582.1:n.10-1291A>C
NM_006819.3:c.10-1291A>C MANE Select	NP_006810.1:n.10-1291A>C
NM_001282652.2:c.151-1291A>C	NP_001269581.1:n.151-1291A>C