Canonical Allele Identifier: CA391934413

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643699C>T (hg19) ; chr15:g.38351498C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351498C>T , CM000677.2:g.38351498C>T	GRCh38
NC_000015.9:g.38643699C>T , CM000677.1:g.38643699C>T	GRCh37
NC_000015.8:g.36430991C>T	NCBI36
NG_008980.1:g.103648C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1169C>T MANE Select	ENSP00000299084.4:p.Pro390Leu
ENST00000299084.8:c.1169C>T	ENSP00000299084.4:p.Pro390Leu
NM_152594.2:c.1169C>T	NP_689807.1:p.Pro390Leu
XM_005254202.2:c.1205C>T	XP_005254259.1:p.Pro402Leu
XM_005254203.3:c.947C>T	XP_005254260.1:p.Pro316Leu
XM_011521288.1:c.1106C>T	XP_011519590.1:p.Pro369Leu
XM_011521289.1:c.1106C>T	XP_011519591.1:p.Pro369Leu
XM_011521290.1:c.1106C>T	XP_011519592.1:p.Pro369Leu
XM_005254202.3:c.1205C>T	XP_005254259.1:p.Pro402Leu
XM_011521289.3:c.1106C>T	XP_011519591.1:p.Pro369Leu
NM_152594.3:c.1169C>T MANE Select	NP_689807.1:p.Pro390Leu