Canonical Allele Identifier: CA2659569817

Gene: SPR

Linked Data

• gnomAD v4: 2-72891659-T-TGAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72891660_72891661insAGGG , CM000664.2:g.72891660_72891661insAGGG	GRCh38
NC_000002.11:g.73118789_73118790insAGGG , CM000664.1:g.73118789_73118790insAGGG	GRCh37
NC_000002.10:g.72972297_72972298insAGGG	NCBI36
NG_008234.1:g.9278_9279insAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234454.6:c.*123_*124insAGGG MANE Select	ENSP00000234454.5:n.*123_*124insAGGG
ENST00000234454.5:c.*123_*124insAGGG	ENSP00000234454.5:n.*123_*124insAGGG
ENST00000498749.1:n.854_855insAGGG
NM_003124.4:c.*123_*124insAGGG	NP_003115.1:n.*123_*124insAGGG
NM_003124.5:c.*123_*124insAGGG MANE Select	NP_003115.1:n.*123_*124insAGGG