Canonical Allele Identifier: CA357618153

Gene: SPP1

Linked Data

• gnomAD v4: 4-87982492-T-C
• MyVariant Identifiers: chr4:g.88903644T>C (hg19) ; chr4:g.87982492T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982492T>C , CM000666.2:g.87982492T>C	GRCh38
NC_000004.11:g.88903644T>C , CM000666.1:g.88903644T>C	GRCh37
NC_000004.10:g.89122668T>C	NCBI36
NG_030362.1:g.11843T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.418T>C	ENSP00000422973.2:p.Tyr140His
ENST00000614857.5:c.541T>C	ENSP00000477824.2:p.Tyr181His
ENST00000681973.1:n.768T>C
ENST00000682026.1:n.494T>C
ENST00000682448.1:n.2027T>C
ENST00000682554.1:n.1989T>C
ENST00000682599.1:n.3029T>C
ENST00000682627.1:n.461T>C
ENST00000682865.1:n.825T>C
ENST00000683087.1:n.555T>C
ENST00000683168.1:n.1295T>C
ENST00000683620.1:n.1723T>C
ENST00000684106.1:n.2791T>C
ENST00000684450.1:n.1600T>C
ENST00000684710.1:n.1832T>C
ENST00000395080.8:c.541T>C MANE Select	ENSP00000378517.3:p.Tyr181His
ENST00000237623.11:c.499T>C	ENSP00000237623.7:p.Tyr167His
ENST00000360804.4:c.460T>C	ENSP00000354042.4:p.Tyr154His
ENST00000395080.7:c.541T>C	ENSP00000378517.3:p.Tyr181His
ENST00000508233.5:c.418T>C	ENSP00000422973.1:p.Tyr140His
ENST00000509659.5:n.830T>C
ENST00000614857.4:c.475T>C	ENSP00000477824.1:p.Tyr159His
NM_000582.2:c.499T>C	NP_000573.1:p.Tyr167His
NM_001040058.1:c.541T>C	NP_001035147.1:p.Tyr181His
NM_001040060.1:c.460T>C	NP_001035149.1:p.Tyr154His
NM_001251829.1:c.418T>C	NP_001238758.1:p.Tyr140His
NM_001251830.1:c.580T>C	NP_001238759.1:p.Tyr194His
NM_001040058.2:c.541T>C MANE Select	NP_001035147.1:p.Tyr181His
NM_000582.3:c.499T>C	NP_000573.1:p.Tyr167His
NM_001040060.2:c.460T>C	NP_001035149.1:p.Tyr154His
NM_001251829.2:c.418T>C	NP_001238758.1:p.Tyr140His
NM_001251830.2:c.580T>C	NP_001238759.1:p.Tyr194His