Canonical Allele Identifier: CA223827773

Gene: STIP1

Linked Data

• dbSNP Id: rs549191434
• gnomAD v3: 11-64196255-G-C
• gnomAD v4: 11-64196255-G-C
• MyVariant Identifiers: chr11:g.63963727G>C (hg19) ; chr11:g.64196255G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196255G>C , CM000673.2:g.64196255G>C	GRCh38
NC_000011.9:g.63963727G>C , CM000673.1:g.63963727G>C	GRCh37
NC_000011.8:g.63720303G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.672+442G>C MANE Select	ENSP00000305958.5:n.672+442G>C
ENST00000305218.8:c.672+442G>C	ENSP00000305958.4:n.672+442G>C
ENST00000358794.9:c.813+442G>C	ENSP00000351646.5:n.813+442G>C
ENST00000536973.5:c.361+1925G>C	ENSP00000441036.1:n.361+1925G>C
ENST00000538945.5:c.600+442G>C	ENSP00000445957.1:n.600+442G>C
NM_001282652.1:c.813+442G>C	NP_001269581.1:n.813+442G>C
NM_001282653.1:c.600+442G>C	NP_001269582.1:n.600+442G>C
NM_006819.2:c.672+442G>C	NP_006810.1:n.672+442G>C
NM_001282653.2:c.600+442G>C	NP_001269582.1:n.600+442G>C
NM_006819.3:c.672+442G>C MANE Select	NP_006810.1:n.672+442G>C
NM_001282652.2:c.813+442G>C	NP_001269581.1:n.813+442G>C