Canonical Allele Identifier: CA489922855

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38641688A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38349487A>C , CM000677.2:g.38349487A>C	GRCh38
NC_000015.9:g.38641688A>C , CM000677.1:g.38641688A>C	GRCh37
NC_000015.8:g.36428980A>C	NCBI36
NG_008980.1:g.101637A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.648A>C MANE Select	ENSP00000299084.4:p.Ile216=
ENST00000299084.8:c.648A>C	ENSP00000299084.4:p.Ile216=
NM_152594.2:c.648A>C	NP_689807.1:p.Ile216=
XM_005254202.2:c.684A>C	XP_005254259.1:p.Ile228=
XM_005254203.3:c.426A>C	XP_005254260.1:p.Ile142=
XM_011521288.1:c.585A>C	XP_011519590.1:p.Ile195=
XM_011521289.1:c.585A>C	XP_011519591.1:p.Ile195=
XM_011521290.1:c.585A>C	XP_011519592.1:p.Ile195=
XM_005254202.3:c.684A>C	XP_005254259.1:p.Ile228=
XM_011521289.3:c.585A>C	XP_011519591.1:p.Ile195=
NM_152594.3:c.648A>C MANE Select	NP_689807.1:p.Ile216=