Canonical Allele Identifier: CA2675739645

Gene: SPRY4

Linked Data

• gnomAD v4: 5-142314170-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.142314170A>G , CM000667.2:g.142314170A>G	GRCh38
NC_000005.9:g.141693735A>G , CM000667.1:g.141693735A>G	GRCh37
NC_000005.8:g.141673919A>G	NCBI36
NG_034148.1:g.15886T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434127.3:c.*39T>C MANE Select	ENSP00000399468.2:n.*39T>C
ENST00000643792.1:n.1621T>C
ENST00000344120.4:c.*39T>C	ENSP00000344967.4:n.*39T>C
ENST00000434127.2:c.*39T>C	ENSP00000399468.2:n.*39T>C
NM_001127496.1:c.*39T>C	NP_001120968.1:n.*39T>C
NM_001293289.1:c.*39T>C	NP_001280218.1:n.*39T>C
NM_001293290.1:c.*39T>C	NP_001280219.1:n.*39T>C
NM_030964.3:c.*39T>C	NP_112226.2:n.*39T>C
XM_011537685.1:c.*39T>C	XP_011535987.1:n.*39T>C
XM_011537685.3:c.*39T>C	XP_011535987.1:n.*39T>C
XM_017009910.2:c.*39T>C	XP_016865399.1:n.*39T>C
NM_001127496.2:c.*39T>C	NP_001120968.1:n.*39T>C
NM_001293289.2:c.*39T>C	NP_001280218.1:n.*39T>C
NM_001293290.2:c.*39T>C	NP_001280219.1:n.*39T>C
NM_030964.4:c.*39T>C	NP_112226.2:n.*39T>C
NM_001127496.3:c.*39T>C MANE Select	NP_001120968.1:n.*39T>C
NM_001293289.3:c.*39T>C	NP_001280218.1:n.*39T>C
NM_001293290.3:c.*39T>C	NP_001280219.1:n.*39T>C
NM_030964.5:c.*39T>C	NP_112226.2:n.*39T>C