Canonical Allele Identifier: CA391933828

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38591596G>C (hg19) ; chr15:g.38299395G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299395G>C , CM000677.2:g.38299395G>C	GRCh38
NC_000015.9:g.38591596G>C , CM000677.1:g.38591596G>C	GRCh37
NC_000015.8:g.36378888G>C	NCBI36
NG_008980.1:g.51545G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.55G>C MANE Select	ENSP00000299084.4:p.Ala19Pro
ENST00000299084.8:c.55G>C	ENSP00000299084.4:p.Ala19Pro
ENST00000561205.1:n.393G>C
ENST00000561317.1:c.-9G>C	ENSP00000453680.1:n.-9G>C
NM_152594.2:c.55G>C	NP_689807.1:p.Ala19Pro
XM_005254202.2:c.91G>C	XP_005254259.1:p.Ala31Pro
XM_005254203.3:c.-15-22846G>C	XP_005254260.1:n.-15-22846G>C
XM_011521288.1:c.-9G>C	XP_011519590.1:n.-9G>C
XM_011521289.1:c.-9G>C	XP_011519591.1:n.-9G>C
XM_011521290.1:c.-9G>C	XP_011519592.1:n.-9G>C
XM_005254202.3:c.91G>C	XP_005254259.1:p.Ala31Pro
XM_011521289.3:c.-9G>C	XP_011519591.1:n.-9G>C
NM_152594.3:c.55G>C MANE Select	NP_689807.1:p.Ala19Pro