Canonical Allele Identifier: CA489922703

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38299418-C-T
• MyVariant Identifiers: chr15:g.38591619C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299418C>T , CM000677.2:g.38299418C>T	GRCh38
NC_000015.9:g.38591619C>T , CM000677.1:g.38591619C>T	GRCh37
NC_000015.8:g.36378911C>T	NCBI36
NG_008980.1:g.51568C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.78C>T MANE Select	ENSP00000299084.4:p.Asp26=
ENST00000299084.8:c.78C>T	ENSP00000299084.4:p.Asp26=
ENST00000561205.1:n.416C>T
ENST00000561317.1:c.15C>T	ENSP00000453680.1:p.Asp5=
NM_152594.2:c.78C>T	NP_689807.1:p.Asp26=
XM_005254202.2:c.114C>T	XP_005254259.1:p.Asp38=
XM_005254203.3:c.-15-22823C>T	XP_005254260.1:n.-15-22823C>T
XM_011521288.1:c.15C>T	XP_011519590.1:p.Asp5=
XM_011521289.1:c.15C>T	XP_011519591.1:p.Asp5=
XM_011521290.1:c.15C>T	XP_011519592.1:p.Asp5=
XM_005254202.3:c.114C>T	XP_005254259.1:p.Asp38=
XM_011521289.3:c.15C>T	XP_011519591.1:p.Asp5=
NM_152594.3:c.78C>T MANE Select	NP_689807.1:p.Asp26=