Canonical Allele Identifier: CA489922717

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38591640A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299439A>G , CM000677.2:g.38299439A>G	GRCh38
NC_000015.9:g.38591640A>G , CM000677.1:g.38591640A>G	GRCh37
NC_000015.8:g.36378932A>G	NCBI36
NG_008980.1:g.51589A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.99A>G MANE Select	ENSP00000299084.4:p.Pro33=
ENST00000299084.8:c.99A>G	ENSP00000299084.4:p.Pro33=
ENST00000561205.1:n.437A>G
ENST00000561317.1:c.36A>G	ENSP00000453680.1:p.Pro12=
NM_152594.2:c.99A>G	NP_689807.1:p.Pro33=
XM_005254202.2:c.135A>G	XP_005254259.1:p.Pro45=
XM_005254203.3:c.-15-22802A>G	XP_005254260.1:n.-15-22802A>G
XM_011521288.1:c.36A>G	XP_011519590.1:p.Pro12=
XM_011521289.1:c.36A>G	XP_011519591.1:p.Pro12=
XM_011521290.1:c.36A>G	XP_011519592.1:p.Pro12=
XM_005254202.3:c.135A>G	XP_005254259.1:p.Pro45=
XM_011521289.3:c.36A>G	XP_011519591.1:p.Pro12=
NM_152594.3:c.99A>G MANE Select	NP_689807.1:p.Pro33=