Canonical Allele Identifier: CA391933938

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38591618A>T (hg19) ; chr15:g.38299417A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299417A>T , CM000677.2:g.38299417A>T	GRCh38
NC_000015.9:g.38591618A>T , CM000677.1:g.38591618A>T	GRCh37
NC_000015.8:g.36378910A>T	NCBI36
NG_008980.1:g.51567A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.77A>T MANE Select	ENSP00000299084.4:p.Asp26Val
ENST00000299084.8:c.77A>T	ENSP00000299084.4:p.Asp26Val
ENST00000561205.1:n.415A>T
ENST00000561317.1:c.14A>T	ENSP00000453680.1:p.Asp5Val
NM_152594.2:c.77A>T	NP_689807.1:p.Asp26Val
XM_005254202.2:c.113A>T	XP_005254259.1:p.Asp38Val
XM_005254203.3:c.-15-22824A>T	XP_005254260.1:n.-15-22824A>T
XM_011521288.1:c.14A>T	XP_011519590.1:p.Asp5Val
XM_011521289.1:c.14A>T	XP_011519591.1:p.Asp5Val
XM_011521290.1:c.14A>T	XP_011519592.1:p.Asp5Val
XM_005254202.3:c.113A>T	XP_005254259.1:p.Asp38Val
XM_011521289.3:c.14A>T	XP_011519591.1:p.Asp5Val
NM_152594.3:c.77A>T MANE Select	NP_689807.1:p.Asp26Val