Canonical Allele Identifier: CA223827797

Gene: STIP1

Linked Data

• dbSNP Id: rs751159427
• MyVariant Identifiers: chr11:g.63963784C>T (hg19) ; chr11:g.64196312C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196312C>T , CM000673.2:g.64196312C>T	GRCh38
NC_000011.9:g.63963784C>T , CM000673.1:g.63963784C>T	GRCh37
NC_000011.8:g.63720360C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.672+499C>T MANE Select	ENSP00000305958.5:n.672+499C>T
ENST00000305218.8:c.672+499C>T	ENSP00000305958.4:n.672+499C>T
ENST00000358794.9:c.813+499C>T	ENSP00000351646.5:n.813+499C>T
ENST00000536973.5:c.361+1982C>T	ENSP00000441036.1:n.361+1982C>T
ENST00000538945.5:c.600+499C>T	ENSP00000445957.1:n.600+499C>T
NM_001282652.1:c.813+499C>T	NP_001269581.1:n.813+499C>T
NM_001282653.1:c.600+499C>T	NP_001269582.1:n.600+499C>T
NM_006819.2:c.672+499C>T	NP_006810.1:n.672+499C>T
NM_001282653.2:c.600+499C>T	NP_001269582.1:n.600+499C>T
NM_006819.3:c.672+499C>T MANE Select	NP_006810.1:n.672+499C>T
NM_001282652.2:c.813+499C>T	NP_001269581.1:n.813+499C>T