Canonical Allele Identifier: CA938815242

Gene: STIP1

Linked Data

• dbSNP Id: rs1946148786
• gnomAD v3: 11-64196260-A-T
• gnomAD v4: 11-64196260-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196260A>T , CM000673.2:g.64196260A>T	GRCh38
NC_000011.9:g.63963732A>T , CM000673.1:g.63963732A>T	GRCh37
NC_000011.8:g.63720308A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.672+447A>T MANE Select	ENSP00000305958.5:n.672+447A>T
ENST00000305218.8:c.672+447A>T	ENSP00000305958.4:n.672+447A>T
ENST00000358794.9:c.813+447A>T	ENSP00000351646.5:n.813+447A>T
ENST00000536973.5:c.361+1930A>T	ENSP00000441036.1:n.361+1930A>T
ENST00000538945.5:c.600+447A>T	ENSP00000445957.1:n.600+447A>T
NM_001282652.1:c.813+447A>T	NP_001269581.1:n.813+447A>T
NM_001282653.1:c.600+447A>T	NP_001269582.1:n.600+447A>T
NM_006819.2:c.672+447A>T	NP_006810.1:n.672+447A>T
NM_001282653.2:c.600+447A>T	NP_001269582.1:n.600+447A>T
NM_006819.3:c.672+447A>T MANE Select	NP_006810.1:n.672+447A>T
NM_001282652.2:c.813+447A>T	NP_001269581.1:n.813+447A>T