Canonical Allele Identifier: CA712595029

Gene: SPRED1

Linked Data

• dbSNP Id: rs1183241164
• gnomAD v3: 15-38322172-T-G
• gnomAD v4: 15-38322172-T-G
• MyVariant Identifiers: chr15:g.38614373T>G (hg19) ; chr15:g.38322172T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38322172T>G , CM000677.2:g.38322172T>G	GRCh38
NC_000015.9:g.38614373T>G , CM000677.1:g.38614373T>G	GRCh37
NC_000015.8:g.36401665T>G	NCBI36
NG_008980.1:g.74322T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.208-69T>G MANE Select	ENSP00000299084.4:n.208-69T>G
ENST00000299084.8:c.208-69T>G	ENSP00000299084.4:n.208-69T>G
ENST00000561205.1:n.546-69T>G
ENST00000561317.1:c.145-69T>G	ENSP00000453680.1:n.145-69T>G
NM_152594.2:c.208-69T>G	NP_689807.1:n.208-69T>G
XM_005254202.2:c.244-69T>G	XP_005254259.1:n.244-69T>G
XM_005254203.3:c.-15-69T>G	XP_005254260.1:n.-15-69T>G
XM_011521288.1:c.145-69T>G	XP_011519590.1:n.145-69T>G
XM_011521289.1:c.145-69T>G	XP_011519591.1:n.145-69T>G
XM_011521290.1:c.145-69T>G	XP_011519592.1:n.145-69T>G
XM_005254202.3:c.244-69T>G	XP_005254259.1:n.244-69T>G
XM_011521289.3:c.145-69T>G	XP_011519591.1:n.145-69T>G
NM_152594.3:c.208-69T>G MANE Select	NP_689807.1:n.208-69T>G