Canonical Allele Identifier: CA1474550965
Gene: SPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1578103943

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87982279A>C , CM000666.2:g.87982279A>C GRCh38
NC_000004.11:g.88903431A>C , CM000666.1:g.88903431A>C GRCh37
NC_000004.10:g.89122455A>C NCBI36
NG_030362.1:g.11630A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000508233.6:c.418-213A>C ENSP00000422973.2:n.418-213A>C
ENST00000614857.5:c.541-213A>C ENSP00000477824.2:n.541-213A>C
ENST00000681973.1:n.768-213A>C
ENST00000682026.1:n.494-213A>C
ENST00000682448.1:n.2027-213A>C
ENST00000682554.1:n.1989-213A>C
ENST00000682599.1:n.3029-213A>C
ENST00000682627.1:n.461-213A>C
ENST00000682865.1:n.825-213A>C
ENST00000683087.1:n.555-213A>C
ENST00000683168.1:n.1295-213A>C
ENST00000683620.1:n.1723-213A>C
ENST00000684106.1:n.2791-213A>C
ENST00000684450.1:n.1600-213A>C
ENST00000684710.1:n.1832-213A>C
ENST00000395080.8:c.541-213A>C MANE Select ENSP00000378517.3:n.541-213A>C
ENST00000237623.11:c.499-213A>C ENSP00000237623.7:n.499-213A>C
ENST00000360804.4:c.460-213A>C ENSP00000354042.4:n.460-213A>C
ENST00000395080.7:c.541-213A>C ENSP00000378517.3:n.541-213A>C
ENST00000508233.5:c.418-213A>C ENSP00000422973.1:n.418-213A>C
ENST00000509659.5:n.830-213A>C
ENST00000614857.4:c.475-213A>C ENSP00000477824.1:n.475-213A>C
NM_000582.2:c.499-213A>C NP_000573.1:n.499-213A>C
NM_001040058.1:c.541-213A>C NP_001035147.1:n.541-213A>C
NM_001040060.1:c.460-213A>C NP_001035149.1:n.460-213A>C
NM_001251829.1:c.418-213A>C NP_001238758.1:n.418-213A>C
NM_001251830.1:c.580-213A>C NP_001238759.1:n.580-213A>C
NM_001040058.2:c.541-213A>C MANE Select NP_001035147.1:n.541-213A>C
NM_000582.3:c.499-213A>C NP_000573.1:n.499-213A>C
NM_001040060.2:c.460-213A>C NP_001035149.1:n.460-213A>C
NM_001251829.2:c.418-213A>C NP_001238758.1:n.418-213A>C
NM_001251830.2:c.580-213A>C NP_001238759.1:n.580-213A>C