Canonical Allele Identifier: CA7470267

Gene: SPRED1

Linked Data

• dbSNP Id: rs772254530
• ExAC: 15:38643898 T / TATA
• gnomAD v2: 15-38643898-T-TATA
• MyVariant Identifiers: chr15:g.38643898_38643899insATA (hg19) ; chr15:g.38351697_38351698insATA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351697_38351698insATA , CM000677.2:g.38351697_38351698insATA	GRCh38
NC_000015.9:g.38643898_38643899insATA , CM000677.1:g.38643898_38643899insATA	GRCh37
NC_000015.8:g.36431190_36431191insATA	NCBI36
NG_008980.1:g.103847_103848insATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*33_*34insATA MANE Select	ENSP00000299084.4:n.*33_*34insATA
ENST00000299084.8:c.*33_*34insATA	ENSP00000299084.4:n.*33_*34insATA
NM_152594.2:c.*33_*34insATA	NP_689807.1:n.*33_*34insATA
XM_005254202.2:c.*33_*34insATA	XP_005254259.1:n.*33_*34insATA
XM_005254203.3:c.*33_*34insATA	XP_005254260.1:n.*33_*34insATA
XM_011521288.1:c.*33_*34insATA	XP_011519590.1:n.*33_*34insATA
XM_011521289.1:c.*33_*34insATA	XP_011519591.1:n.*33_*34insATA
XM_011521290.1:c.*33_*34insATA	XP_011519592.1:n.*33_*34insATA
XM_005254202.3:c.*33_*34insATA	XP_005254259.1:n.*33_*34insATA
XM_011521289.3:c.*33_*34insATA	XP_011519591.1:n.*33_*34insATA
NM_152594.3:c.*33_*34insATA MANE Select	NP_689807.1:n.*33_*34insATA