Canonical Allele Identifier: CA391933795

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643547G>T (hg19) ; chr15:g.38351346G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351346G>T , CM000677.2:g.38351346G>T	GRCh38
NC_000015.9:g.38643547G>T , CM000677.1:g.38643547G>T	GRCh37
NC_000015.8:g.36430839G>T	NCBI36
NG_008980.1:g.103496G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1017G>T MANE Select	ENSP00000299084.4:p.Gln339His
ENST00000299084.8:c.1017G>T	ENSP00000299084.4:p.Gln339His
NM_152594.2:c.1017G>T	NP_689807.1:p.Gln339His
XM_005254202.2:c.1053G>T	XP_005254259.1:p.Gln351His
XM_005254203.3:c.795G>T	XP_005254260.1:p.Gln265His
XM_011521288.1:c.954G>T	XP_011519590.1:p.Gln318His
XM_011521289.1:c.954G>T	XP_011519591.1:p.Gln318His
XM_011521290.1:c.954G>T	XP_011519592.1:p.Gln318His
XM_005254202.3:c.1053G>T	XP_005254259.1:p.Gln351His
XM_011521289.3:c.954G>T	XP_011519591.1:p.Gln318His
NM_152594.3:c.1017G>T MANE Select	NP_689807.1:p.Gln339His