Canonical Allele Identifier: CA6599511

Gene: SP7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53328587C>T , CM000674.2:g.53328587C>T	GRCh38
NC_000012.11:g.53722371C>T , CM000674.1:g.53722371C>T	GRCh37
NC_000012.10:g.52008638C>T	NCBI36
NG_023391.1:g.12634G>A
NG_023391.2:g.21207G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001173467.3:c.855G>A MANE Select	NP_001166938.1:p.Ala285=
ENST00000536324.4:c.855G>A MANE Select	ENSP00000443827.2:p.Ala285=
NM_001173467.2:c.855G>A	NP_001166938.1:p.Ala285=
NM_001300837.1:c.801G>A	NP_001287766.1:p.Ala267=
NM_001300837.2:c.801G>A	NP_001287766.1:p.Ala267=
NM_152860.1:c.855G>A	NP_690599.1:p.Ala285=
NM_152860.2:c.855G>A	NP_690599.1:p.Ala285=
ENST00000303846.3:c.855G>A	ENSP00000302812.3:p.Ala285=
ENST00000536324.3:c.855G>A	ENSP00000443827.2:p.Ala285=
ENST00000537210.2:c.801G>A	ENSP00000441367.2:p.Ala267=
ENST00000547755.1:c.801G>A	ENSP00000449355.1:p.Ala267=
XM_011537900.1:c.801G>A	XP_011536202.1:p.Ala267=
XM_011537900.2:c.801G>A	XP_011536202.1:p.Ala267=
XM_011537901.1:c.801G>A	XP_011536203.1:p.Ala267=