Canonical Allele Identifier: CA489921681

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38253200-G-T
• MyVariant Identifiers: chr15:g.38545401G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253200G>T , CM000677.2:g.38253200G>T	GRCh38
NC_000015.9:g.38545401G>T , CM000677.1:g.38545401G>T	GRCh37
NC_000015.8:g.36332693G>T	NCBI36
NG_008980.1:g.5350G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.15G>T MANE Select	ENSP00000299084.4:p.Thr5=
ENST00000299084.8:c.15G>T	ENSP00000299084.4:p.Thr5=
ENST00000561205.1:n.353G>T
ENST00000561317.1:c.-113G>T	ENSP00000453680.1:n.-113G>T
NM_152594.2:c.15G>T	NP_689807.1:p.Thr5=
XM_005254202.2:c.15G>T	XP_005254259.1:p.Thr5=
XM_005254203.3:c.-33G>T	XP_005254260.1:n.-33G>T
XM_005254202.3:c.15G>T	XP_005254259.1:p.Thr5=
XR_001751484.1:n.87+367C>A
NM_152594.3:c.15G>T MANE Select	NP_689807.1:p.Thr5=