Canonical Allele Identifier: CA391933446

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643404T>A (hg19) ; chr15:g.38351203T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351203T>A , CM000677.2:g.38351203T>A	GRCh38
NC_000015.9:g.38643404T>A , CM000677.1:g.38643404T>A	GRCh37
NC_000015.8:g.36430696T>A	NCBI36
NG_008980.1:g.103353T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.874T>A MANE Select	ENSP00000299084.4:p.Tyr292Asn
ENST00000299084.8:c.874T>A	ENSP00000299084.4:p.Tyr292Asn
NM_152594.2:c.874T>A	NP_689807.1:p.Tyr292Asn
XM_005254202.2:c.910T>A	XP_005254259.1:p.Tyr304Asn
XM_005254203.3:c.652T>A	XP_005254260.1:p.Tyr218Asn
XM_011521288.1:c.811T>A	XP_011519590.1:p.Tyr271Asn
XM_011521289.1:c.811T>A	XP_011519591.1:p.Tyr271Asn
XM_011521290.1:c.811T>A	XP_011519592.1:p.Tyr271Asn
XM_005254202.3:c.910T>A	XP_005254259.1:p.Tyr304Asn
XM_011521289.3:c.811T>A	XP_011519591.1:p.Tyr271Asn
NM_152594.3:c.874T>A MANE Select	NP_689807.1:p.Tyr292Asn