Canonical Allele Identifier: CA391933449

Gene: SPRED1

Linked Data

• COSMIC: COSM4054223
• MyVariant Identifiers: chr15:g.38643405A>T (hg19) ; chr15:g.38351204A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351204A>T , CM000677.2:g.38351204A>T	GRCh38
NC_000015.9:g.38643405A>T , CM000677.1:g.38643405A>T	GRCh37
NC_000015.8:g.36430697A>T	NCBI36
NG_008980.1:g.103354A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.875A>T MANE Select	ENSP00000299084.4:p.Tyr292Phe
ENST00000299084.8:c.875A>T	ENSP00000299084.4:p.Tyr292Phe
NM_152594.2:c.875A>T	NP_689807.1:p.Tyr292Phe
XM_005254202.2:c.911A>T	XP_005254259.1:p.Tyr304Phe
XM_005254203.3:c.653A>T	XP_005254260.1:p.Tyr218Phe
XM_011521288.1:c.812A>T	XP_011519590.1:p.Tyr271Phe
XM_011521289.1:c.812A>T	XP_011519591.1:p.Tyr271Phe
XM_011521290.1:c.812A>T	XP_011519592.1:p.Tyr271Phe
XM_005254202.3:c.911A>T	XP_005254259.1:p.Tyr304Phe
XM_011521289.3:c.812A>T	XP_011519591.1:p.Tyr271Phe
NM_152594.3:c.875A>T MANE Select	NP_689807.1:p.Tyr292Phe