Canonical Allele Identifier: CA391933929

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38299416-G-T
• MyVariant Identifiers: chr15:g.38591617G>T (hg19) ; chr15:g.38299416G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299416G>T , CM000677.2:g.38299416G>T	GRCh38
NC_000015.9:g.38591617G>T , CM000677.1:g.38591617G>T	GRCh37
NC_000015.8:g.36378909G>T	NCBI36
NG_008980.1:g.51566G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.76G>T MANE Select	ENSP00000299084.4:p.Asp26Tyr
ENST00000299084.8:c.76G>T	ENSP00000299084.4:p.Asp26Tyr
ENST00000561205.1:n.414G>T
ENST00000561317.1:c.13G>T	ENSP00000453680.1:p.Asp5Tyr
NM_152594.2:c.76G>T	NP_689807.1:p.Asp26Tyr
XM_005254202.2:c.112G>T	XP_005254259.1:p.Asp38Tyr
XM_005254203.3:c.-15-22825G>T	XP_005254260.1:n.-15-22825G>T
XM_011521288.1:c.13G>T	XP_011519590.1:p.Asp5Tyr
XM_011521289.1:c.13G>T	XP_011519591.1:p.Asp5Tyr
XM_011521290.1:c.13G>T	XP_011519592.1:p.Asp5Tyr
XM_005254202.3:c.112G>T	XP_005254259.1:p.Asp38Tyr
XM_011521289.3:c.13G>T	XP_011519591.1:p.Asp5Tyr
NM_152594.3:c.76G>T MANE Select	NP_689807.1:p.Asp26Tyr