Canonical Allele Identifier: CA391933837

Gene: SPRED1

Linked Data

• COSMIC: COSM4054225
• MyVariant Identifiers: chr15:g.38643558A>G (hg19) ; chr15:g.38351357A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351357A>G , CM000677.2:g.38351357A>G	GRCh38
NC_000015.9:g.38643558A>G , CM000677.1:g.38643558A>G	GRCh37
NC_000015.8:g.36430850A>G	NCBI36
NG_008980.1:g.103507A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1028A>G MANE Select	ENSP00000299084.4:p.Asn343Ser
ENST00000299084.8:c.1028A>G	ENSP00000299084.4:p.Asn343Ser
NM_152594.2:c.1028A>G	NP_689807.1:p.Asn343Ser
XM_005254202.2:c.1064A>G	XP_005254259.1:p.Asn355Ser
XM_005254203.3:c.806A>G	XP_005254260.1:p.Asn269Ser
XM_011521288.1:c.965A>G	XP_011519590.1:p.Asn322Ser
XM_011521289.1:c.965A>G	XP_011519591.1:p.Asn322Ser
XM_011521290.1:c.965A>G	XP_011519592.1:p.Asn322Ser
XM_005254202.3:c.1064A>G	XP_005254259.1:p.Asn355Ser
XM_011521289.3:c.965A>G	XP_011519591.1:p.Asn322Ser
NM_152594.3:c.1028A>G MANE Select	NP_689807.1:p.Asn343Ser