Canonical Allele Identifier: CA1474550960

Gene: SPP1

Linked Data

• dbSNP Id: rs1725679786

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982265_87982266insGG , CM000666.2:g.87982265_87982266insGG	GRCh38
NC_000004.11:g.88903417_88903418insGG , CM000666.1:g.88903417_88903418insGG	GRCh37
NC_000004.10:g.89122441_89122442insGG	NCBI36
NG_030362.1:g.11616_11617insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.418-227_418-226insGG	ENSP00000422973.2:n.418-227_418-226insGG
ENST00000614857.5:c.541-227_541-226insGG	ENSP00000477824.2:n.541-227_541-226insGG
ENST00000681973.1:n.768-227_768-226insGG
ENST00000682026.1:n.494-227_494-226insGG
ENST00000682448.1:n.2027-227_2027-226insGG
ENST00000682554.1:n.1989-227_1989-226insGG
ENST00000682599.1:n.3029-227_3029-226insGG
ENST00000682627.1:n.461-227_461-226insGG
ENST00000682865.1:n.825-227_825-226insGG
ENST00000683087.1:n.555-227_555-226insGG
ENST00000683168.1:n.1295-227_1295-226insGG
ENST00000683620.1:n.1723-227_1723-226insGG
ENST00000684106.1:n.2791-227_2791-226insGG
ENST00000684450.1:n.1600-227_1600-226insGG
ENST00000684710.1:n.1832-227_1832-226insGG
ENST00000395080.8:c.541-227_541-226insGG MANE Select	ENSP00000378517.3:n.541-227_541-226insGG
ENST00000237623.11:c.499-227_499-226insGG	ENSP00000237623.7:n.499-227_499-226insGG
ENST00000360804.4:c.460-227_460-226insGG	ENSP00000354042.4:n.460-227_460-226insGG
ENST00000395080.7:c.541-227_541-226insGG	ENSP00000378517.3:n.541-227_541-226insGG
ENST00000508233.5:c.418-227_418-226insGG	ENSP00000422973.1:n.418-227_418-226insGG
ENST00000509659.5:n.830-227_830-226insGG
ENST00000614857.4:c.475-227_475-226insGG	ENSP00000477824.1:n.475-227_475-226insGG
NM_000582.2:c.499-227_499-226insGG	NP_000573.1:n.499-227_499-226insGG
NM_001040058.1:c.541-227_541-226insGG	NP_001035147.1:n.541-227_541-226insGG
NM_001040060.1:c.460-227_460-226insGG	NP_001035149.1:n.460-227_460-226insGG
NM_001251829.1:c.418-227_418-226insGG	NP_001238758.1:n.418-227_418-226insGG
NM_001251830.1:c.580-227_580-226insGG	NP_001238759.1:n.580-227_580-226insGG
NM_001040058.2:c.541-227_541-226insGG MANE Select	NP_001035147.1:n.541-227_541-226insGG
NM_000582.3:c.499-227_499-226insGG	NP_000573.1:n.499-227_499-226insGG
NM_001040060.2:c.460-227_460-226insGG	NP_001035149.1:n.460-227_460-226insGG
NM_001251829.2:c.418-227_418-226insGG	NP_001238758.1:n.418-227_418-226insGG
NM_001251830.2:c.580-227_580-226insGG	NP_001238759.1:n.580-227_580-226insGG