Canonical Allele Identifier: CA391934163

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643638C>G (hg19) ; chr15:g.38351437C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351437C>G , CM000677.2:g.38351437C>G	GRCh38
NC_000015.9:g.38643638C>G , CM000677.1:g.38643638C>G	GRCh37
NC_000015.8:g.36430930C>G	NCBI36
NG_008980.1:g.103587C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1108C>G MANE Select	ENSP00000299084.4:p.Leu370Val
ENST00000299084.8:c.1108C>G	ENSP00000299084.4:p.Leu370Val
NM_152594.2:c.1108C>G	NP_689807.1:p.Leu370Val
XM_005254202.2:c.1144C>G	XP_005254259.1:p.Leu382Val
XM_005254203.3:c.886C>G	XP_005254260.1:p.Leu296Val
XM_011521288.1:c.1045C>G	XP_011519590.1:p.Leu349Val
XM_011521289.1:c.1045C>G	XP_011519591.1:p.Leu349Val
XM_011521290.1:c.1045C>G	XP_011519592.1:p.Leu349Val
XM_005254202.3:c.1144C>G	XP_005254259.1:p.Leu382Val
XM_011521289.3:c.1045C>G	XP_011519591.1:p.Leu349Val
NM_152594.3:c.1108C>G MANE Select	NP_689807.1:p.Leu370Val