Canonical Allele Identifier: CA357618286

Gene: SPP1

Linked Data

• gnomAD v4: 4-87982523-C-T
• MyVariant Identifiers: chr4:g.88903675C>T (hg19) ; chr4:g.87982523C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982523C>T , CM000666.2:g.87982523C>T	GRCh38
NC_000004.11:g.88903675C>T , CM000666.1:g.88903675C>T	GRCh37
NC_000004.10:g.89122699C>T	NCBI36
NG_030362.1:g.11874C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.449C>T	ENSP00000422973.2:p.Ser150Leu
ENST00000614857.5:c.572C>T	ENSP00000477824.2:p.Ser191Leu
ENST00000681973.1:n.799C>T
ENST00000682026.1:n.525C>T
ENST00000682448.1:n.2058C>T
ENST00000682554.1:n.2020C>T
ENST00000682599.1:n.3060C>T
ENST00000682627.1:n.492C>T
ENST00000682865.1:n.856C>T
ENST00000683087.1:n.586C>T
ENST00000683168.1:n.1326C>T
ENST00000683620.1:n.1754C>T
ENST00000684106.1:n.2822C>T
ENST00000684450.1:n.1631C>T
ENST00000684710.1:n.1863C>T
ENST00000395080.8:c.572C>T MANE Select	ENSP00000378517.3:p.Ser191Leu
ENST00000237623.11:c.530C>T	ENSP00000237623.7:p.Ser177Leu
ENST00000360804.4:c.491C>T	ENSP00000354042.4:p.Ser164Leu
ENST00000395080.7:c.572C>T	ENSP00000378517.3:p.Ser191Leu
ENST00000508233.5:c.449C>T	ENSP00000422973.1:p.Ser150Leu
ENST00000509659.5:n.861C>T
ENST00000614857.4:c.506C>T	ENSP00000477824.1:p.Ser169Leu
NM_000582.2:c.530C>T	NP_000573.1:p.Ser177Leu
NM_001040058.1:c.572C>T	NP_001035147.1:p.Ser191Leu
NM_001040060.1:c.491C>T	NP_001035149.1:p.Ser164Leu
NM_001251829.1:c.449C>T	NP_001238758.1:p.Ser150Leu
NM_001251830.1:c.611C>T	NP_001238759.1:p.Ser204Leu
NM_001040058.2:c.572C>T MANE Select	NP_001035147.1:p.Ser191Leu
NM_000582.3:c.530C>T	NP_000573.1:p.Ser177Leu
NM_001040060.2:c.491C>T	NP_001035149.1:p.Ser164Leu
NM_001251829.2:c.449C>T	NP_001238758.1:p.Ser150Leu
NM_001251830.2:c.611C>T	NP_001238759.1:p.Ser204Leu