Canonical Allele Identifier: CA391933902

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38591611C>G (hg19) ; chr15:g.38299410C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299410C>G , CM000677.2:g.38299410C>G	GRCh38
NC_000015.9:g.38591611C>G , CM000677.1:g.38591611C>G	GRCh37
NC_000015.8:g.36378903C>G	NCBI36
NG_008980.1:g.51560C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.70C>G MANE Select	ENSP00000299084.4:p.Arg24Gly
ENST00000299084.8:c.70C>G	ENSP00000299084.4:p.Arg24Gly
ENST00000561205.1:n.408C>G
ENST00000561317.1:c.7C>G	ENSP00000453680.1:p.Arg3Gly
NM_152594.2:c.70C>G	NP_689807.1:p.Arg24Gly
XM_005254202.2:c.106C>G	XP_005254259.1:p.Arg36Gly
XM_005254203.3:c.-15-22831C>G	XP_005254260.1:n.-15-22831C>G
XM_011521288.1:c.7C>G	XP_011519590.1:p.Arg3Gly
XM_011521289.1:c.7C>G	XP_011519591.1:p.Arg3Gly
XM_011521290.1:c.7C>G	XP_011519592.1:p.Arg3Gly
XM_005254202.3:c.106C>G	XP_005254259.1:p.Arg36Gly
XM_011521289.3:c.7C>G	XP_011519591.1:p.Arg3Gly
NM_152594.3:c.70C>G MANE Select	NP_689807.1:p.Arg24Gly