Canonical Allele Identifier: CA391934571

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643741G>C (hg19) ; chr15:g.38351540G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351540G>C , CM000677.2:g.38351540G>C	GRCh38
NC_000015.9:g.38643741G>C , CM000677.1:g.38643741G>C	GRCh37
NC_000015.8:g.36431033G>C	NCBI36
NG_008980.1:g.103690G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1211G>C MANE Select	ENSP00000299084.4:p.Trp404Ser
ENST00000299084.8:c.1211G>C	ENSP00000299084.4:p.Trp404Ser
NM_152594.2:c.1211G>C	NP_689807.1:p.Trp404Ser
XM_005254202.2:c.1247G>C	XP_005254259.1:p.Trp416Ser
XM_005254203.3:c.989G>C	XP_005254260.1:p.Trp330Ser
XM_011521288.1:c.1148G>C	XP_011519590.1:p.Trp383Ser
XM_011521289.1:c.1148G>C	XP_011519591.1:p.Trp383Ser
XM_011521290.1:c.1148G>C	XP_011519592.1:p.Trp383Ser
XM_005254202.3:c.1247G>C	XP_005254259.1:p.Trp416Ser
XM_011521289.3:c.1148G>C	XP_011519591.1:p.Trp383Ser
NM_152594.3:c.1211G>C MANE Select	NP_689807.1:p.Trp404Ser