Canonical Allele Identifier: CA391933358

Gene: SPRED1

Linked Data

• dbSNP Id: rs904563789
• MyVariant Identifiers: chr15:g.38643366G>T (hg19) ; chr15:g.38351165G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351165G>T , CM000677.2:g.38351165G>T	GRCh38
NC_000015.9:g.38643366G>T , CM000677.1:g.38643366G>T	GRCh37
NC_000015.8:g.36430658G>T	NCBI36
NG_008980.1:g.103315G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.836G>T MANE Select	ENSP00000299084.4:p.Ser279Ile
ENST00000299084.8:c.836G>T	ENSP00000299084.4:p.Ser279Ile
NM_152594.2:c.836G>T	NP_689807.1:p.Ser279Ile
XM_005254202.2:c.872G>T	XP_005254259.1:p.Ser291Ile
XM_005254203.3:c.614G>T	XP_005254260.1:p.Ser205Ile
XM_011521288.1:c.773G>T	XP_011519590.1:p.Ser258Ile
XM_011521289.1:c.773G>T	XP_011519591.1:p.Ser258Ile
XM_011521290.1:c.773G>T	XP_011519592.1:p.Ser258Ile
XM_005254202.3:c.872G>T	XP_005254259.1:p.Ser291Ile
XM_011521289.3:c.773G>T	XP_011519591.1:p.Ser258Ile
NM_152594.3:c.836G>T MANE Select	NP_689807.1:p.Ser279Ile