Canonical Allele Identifier: CA712577488

Gene: SPRED1

Linked Data

• dbSNP Id: rs1365570456
• gnomAD v3: 15-38352238-G-GTATA
• gnomAD v4: 15-38352238-G-GTATA
• MyVariant Identifiers: chr15:g.38644439_38644440insTATA (hg19) ; chr15:g.38352238_38352239insTATA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38352240_38352241insTATA , CM000677.2:g.38352240_38352241insTATA	GRCh38
NC_000015.9:g.38644441_38644442insTATA , CM000677.1:g.38644441_38644442insTATA	GRCh37
NC_000015.8:g.36431733_36431734insTATA	NCBI36
NG_008980.1:g.104390_104391insTATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*576_*577insTATA MANE Select	ENSP00000299084.4:n.*576_*577insTATA
ENST00000299084.8:c.*576_*577insTATA	ENSP00000299084.4:n.*576_*577insTATA
NM_152594.2:c.*576_*577insTATA	NP_689807.1:n.*576_*577insTATA
XM_005254202.2:c.*576_*577insTATA	XP_005254259.1:n.*576_*577insTATA
XM_005254203.3:c.*576_*577insTATA	XP_005254260.1:n.*576_*577insTATA
XM_011521288.1:c.*576_*577insTATA	XP_011519590.1:n.*576_*577insTATA
XM_011521289.1:c.*576_*577insTATA	XP_011519591.1:n.*576_*577insTATA
XM_011521290.1:c.*576_*577insTATA	XP_011519592.1:n.*576_*577insTATA
XM_005254202.3:c.*576_*577insTATA	XP_005254259.1:n.*576_*577insTATA
XM_011521289.3:c.*576_*577insTATA	XP_011519591.1:n.*576_*577insTATA
NM_152594.3:c.*576_*577insTATA MANE Select	NP_689807.1:n.*576_*577insTATA