Canonical Allele Identifier: CA391933145

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643275A>T (hg19) ; chr15:g.38351074A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351074A>T , CM000677.2:g.38351074A>T	GRCh38
NC_000015.9:g.38643275A>T , CM000677.1:g.38643275A>T	GRCh37
NC_000015.8:g.36430567A>T	NCBI36
NG_008980.1:g.103224A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.745A>T MANE Select	ENSP00000299084.4:p.Asn249Tyr
ENST00000299084.8:c.745A>T	ENSP00000299084.4:p.Asn249Tyr
NM_152594.2:c.745A>T	NP_689807.1:p.Asn249Tyr
XM_005254202.2:c.781A>T	XP_005254259.1:p.Asn261Tyr
XM_005254203.3:c.523A>T	XP_005254260.1:p.Asn175Tyr
XM_011521288.1:c.682A>T	XP_011519590.1:p.Asn228Tyr
XM_011521289.1:c.682A>T	XP_011519591.1:p.Asn228Tyr
XM_011521290.1:c.682A>T	XP_011519592.1:p.Asn228Tyr
XM_005254202.3:c.781A>T	XP_005254259.1:p.Asn261Tyr
XM_011521289.3:c.682A>T	XP_011519591.1:p.Asn228Tyr
NM_152594.3:c.745A>T MANE Select	NP_689807.1:p.Asn249Tyr