Canonical Allele Identifier: CA391931832

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38545405A>T (hg19) ; chr15:g.38253204A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253204A>T , CM000677.2:g.38253204A>T	GRCh38
NC_000015.9:g.38545405A>T , CM000677.1:g.38545405A>T	GRCh37
NC_000015.8:g.36332697A>T	NCBI36
NG_008980.1:g.5354A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.19A>T MANE Select	ENSP00000299084.4:p.Thr7Ser
ENST00000299084.8:c.19A>T	ENSP00000299084.4:p.Thr7Ser
ENST00000561205.1:n.357A>T
ENST00000561317.1:c.-109A>T	ENSP00000453680.1:n.-109A>T
NM_152594.2:c.19A>T	NP_689807.1:p.Thr7Ser
XM_005254202.2:c.19A>T	XP_005254259.1:p.Thr7Ser
XM_005254203.3:c.-29A>T	XP_005254260.1:n.-29A>T
XM_005254202.3:c.19A>T	XP_005254259.1:p.Thr7Ser
XR_001751484.1:n.87+363T>A
NM_152594.3:c.19A>T MANE Select	NP_689807.1:p.Thr7Ser