Canonical Allele Identifier: CA3485442

Gene: SPRY4

Linked Data

• dbSNP Id: rs769196353
• ExAC: 5:141693770 A / T
• gnomAD v2: 5-141693770-A-T
• gnomAD v4: 5-142314205-A-T
• MyVariant Identifiers: chr5:g.141693770A>T (hg19) ; chr5:g.142314205A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.142314205A>T , CM000667.2:g.142314205A>T	GRCh38
NC_000005.9:g.141693770A>T , CM000667.1:g.141693770A>T	GRCh37
NC_000005.8:g.141673954A>T	NCBI36
NG_034148.1:g.15851T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434127.3:c.*4T>A MANE Select	ENSP00000399468.2:n.*4T>A
ENST00000643792.1:n.1586T>A
ENST00000344120.4:c.*4T>A	ENSP00000344967.4:n.*4T>A
ENST00000434127.2:c.*4T>A	ENSP00000399468.2:n.*4T>A
NM_001127496.1:c.*4T>A	NP_001120968.1:n.*4T>A
NM_001293289.1:c.*4T>A	NP_001280218.1:n.*4T>A
NM_001293290.1:c.*4T>A	NP_001280219.1:n.*4T>A
NM_030964.3:c.*4T>A	NP_112226.2:n.*4T>A
XM_011537685.1:c.*4T>A	XP_011535987.1:n.*4T>A
XM_011537685.3:c.*4T>A	XP_011535987.1:n.*4T>A
XM_017009910.2:c.*4T>A	XP_016865399.1:n.*4T>A
NM_001127496.2:c.*4T>A	NP_001120968.1:n.*4T>A
NM_001293289.2:c.*4T>A	NP_001280218.1:n.*4T>A
NM_001293290.2:c.*4T>A	NP_001280219.1:n.*4T>A
NM_030964.4:c.*4T>A	NP_112226.2:n.*4T>A
NM_001127496.3:c.*4T>A MANE Select	NP_001120968.1:n.*4T>A
NM_001293289.3:c.*4T>A	NP_001280218.1:n.*4T>A
NM_001293290.3:c.*4T>A	NP_001280219.1:n.*4T>A
NM_030964.5:c.*4T>A	NP_112226.2:n.*4T>A