Canonical Allele Identifier: CA391932951

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38641705G>T (hg19) ; chr15:g.38349504G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38349504G>T , CM000677.2:g.38349504G>T	GRCh38
NC_000015.9:g.38641705G>T , CM000677.1:g.38641705G>T	GRCh37
NC_000015.8:g.36428997G>T	NCBI36
NG_008980.1:g.101654G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.665G>T MANE Select	ENSP00000299084.4:p.Ser222Ile
ENST00000299084.8:c.665G>T	ENSP00000299084.4:p.Ser222Ile
NM_152594.2:c.665G>T	NP_689807.1:p.Ser222Ile
XM_005254202.2:c.701G>T	XP_005254259.1:p.Ser234Ile
XM_005254203.3:c.443G>T	XP_005254260.1:p.Ser148Ile
XM_011521288.1:c.602G>T	XP_011519590.1:p.Ser201Ile
XM_011521289.1:c.602G>T	XP_011519591.1:p.Ser201Ile
XM_011521290.1:c.602G>T	XP_011519592.1:p.Ser201Ile
XM_005254202.3:c.701G>T	XP_005254259.1:p.Ser234Ile
XM_011521289.3:c.602G>T	XP_011519591.1:p.Ser201Ile
NM_152594.3:c.665G>T MANE Select	NP_689807.1:p.Ser222Ile