Canonical Allele Identifier: CA391932896

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38641679G>C (hg19) ; chr15:g.38349478G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38349478G>C , CM000677.2:g.38349478G>C	GRCh38
NC_000015.9:g.38641679G>C , CM000677.1:g.38641679G>C	GRCh37
NC_000015.8:g.36428971G>C	NCBI36
NG_008980.1:g.101628G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.639G>C MANE Select	ENSP00000299084.4:p.Gln213His
ENST00000299084.8:c.639G>C	ENSP00000299084.4:p.Gln213His
NM_152594.2:c.639G>C	NP_689807.1:p.Gln213His
XM_005254202.2:c.675G>C	XP_005254259.1:p.Gln225His
XM_005254203.3:c.417G>C	XP_005254260.1:p.Gln139His
XM_011521288.1:c.576G>C	XP_011519590.1:p.Gln192His
XM_011521289.1:c.576G>C	XP_011519591.1:p.Gln192His
XM_011521290.1:c.576G>C	XP_011519592.1:p.Gln192His
XM_005254202.3:c.675G>C	XP_005254259.1:p.Gln225His
XM_011521289.3:c.576G>C	XP_011519591.1:p.Gln192His
NM_152594.3:c.639G>C MANE Select	NP_689807.1:p.Gln213His