Canonical Allele Identifier: CA391934470

Gene: SPRED1

Linked Data

• dbSNP Id: rs991687184
• gnomAD v3: 15-38351513-C-T
• gnomAD v4: 15-38351513-C-T
• MyVariant Identifiers: chr15:g.38643714C>T (hg19) ; chr15:g.38351513C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351513C>T , CM000677.2:g.38351513C>T	GRCh38
NC_000015.9:g.38643714C>T , CM000677.1:g.38643714C>T	GRCh37
NC_000015.8:g.36431006C>T	NCBI36
NG_008980.1:g.103663C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1184C>T MANE Select	ENSP00000299084.4:p.Thr395Ile
ENST00000299084.8:c.1184C>T	ENSP00000299084.4:p.Thr395Ile
NM_152594.2:c.1184C>T	NP_689807.1:p.Thr395Ile
XM_005254202.2:c.1220C>T	XP_005254259.1:p.Thr407Ile
XM_005254203.3:c.962C>T	XP_005254260.1:p.Thr321Ile
XM_011521288.1:c.1121C>T	XP_011519590.1:p.Thr374Ile
XM_011521289.1:c.1121C>T	XP_011519591.1:p.Thr374Ile
XM_011521290.1:c.1121C>T	XP_011519592.1:p.Thr374Ile
XM_005254202.3:c.1220C>T	XP_005254259.1:p.Thr407Ile
XM_011521289.3:c.1121C>T	XP_011519591.1:p.Thr374Ile
NM_152594.3:c.1184C>T MANE Select	NP_689807.1:p.Thr395Ile