Canonical Allele Identifier: CA391933187

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38351092-A-G
• MyVariant Identifiers: chr15:g.38643293A>G (hg19) ; chr15:g.38351092A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351092A>G , CM000677.2:g.38351092A>G	GRCh38
NC_000015.9:g.38643293A>G , CM000677.1:g.38643293A>G	GRCh37
NC_000015.8:g.36430585A>G	NCBI36
NG_008980.1:g.103242A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.763A>G MANE Select	ENSP00000299084.4:p.Ile255Val
ENST00000299084.8:c.763A>G	ENSP00000299084.4:p.Ile255Val
NM_152594.2:c.763A>G	NP_689807.1:p.Ile255Val
XM_005254202.2:c.799A>G	XP_005254259.1:p.Ile267Val
XM_005254203.3:c.541A>G	XP_005254260.1:p.Ile181Val
XM_011521288.1:c.700A>G	XP_011519590.1:p.Ile234Val
XM_011521289.1:c.700A>G	XP_011519591.1:p.Ile234Val
XM_011521290.1:c.700A>G	XP_011519592.1:p.Ile234Val
XM_005254202.3:c.799A>G	XP_005254259.1:p.Ile267Val
XM_011521289.3:c.700A>G	XP_011519591.1:p.Ile234Val
NM_152594.3:c.763A>G MANE Select	NP_689807.1:p.Ile255Val