Canonical Allele Identifier: CA712577569

Gene: SPRED1

Linked Data

• dbSNP Id: rs1370154001
• gnomAD v3: 15-38352337-T-TA
• gnomAD v4: 15-38352337-T-TA
• MyVariant Identifiers: chr15:g.38644538_38644539insA (hg19) ; chr15:g.38352337_38352338insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38352338dup , CM000677.2:g.38352338dup	GRCh38
NC_000015.9:g.38644539dup , CM000677.1:g.38644539dup	GRCh37
NC_000015.8:g.36431831dup	NCBI36
NG_008980.1:g.104488dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*674dup MANE Select	ENSP00000299084.4:n.*674dup
ENST00000299084.8:c.*674dup	ENSP00000299084.4:n.*674dup
NM_152594.2:c.*674dup	NP_689807.1:n.*674dup
XM_005254202.2:c.*674dup	XP_005254259.1:n.*674dup
XM_005254203.3:c.*674dup	XP_005254260.1:n.*674dup
XM_011521288.1:c.*674dup	XP_011519590.1:n.*674dup
XM_011521289.1:c.*674dup	XP_011519591.1:n.*674dup
XM_011521290.1:c.*674dup	XP_011519592.1:n.*674dup
XM_005254202.3:c.*674dup	XP_005254259.1:n.*674dup
XM_011521289.3:c.*674dup	XP_011519591.1:n.*674dup
NM_152594.3:c.*674dup MANE Select	NP_689807.1:n.*674dup