Canonical Allele Identifier: CA2675739656

Gene: SPRY4

Linked Data

• gnomAD v4: 5-142314180-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.142314180G>A , CM000667.2:g.142314180G>A	GRCh38
NC_000005.9:g.141693745G>A , CM000667.1:g.141693745G>A	GRCh37
NC_000005.8:g.141673929G>A	NCBI36
NG_034148.1:g.15876C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434127.3:c.*29C>T MANE Select	ENSP00000399468.2:n.*29C>T
ENST00000643792.1:n.1611C>T
ENST00000344120.4:c.*29C>T	ENSP00000344967.4:n.*29C>T
ENST00000434127.2:c.*29C>T	ENSP00000399468.2:n.*29C>T
NM_001127496.1:c.*29C>T	NP_001120968.1:n.*29C>T
NM_001293289.1:c.*29C>T	NP_001280218.1:n.*29C>T
NM_001293290.1:c.*29C>T	NP_001280219.1:n.*29C>T
NM_030964.3:c.*29C>T	NP_112226.2:n.*29C>T
XM_011537685.1:c.*29C>T	XP_011535987.1:n.*29C>T
XM_011537685.3:c.*29C>T	XP_011535987.1:n.*29C>T
XM_017009910.2:c.*29C>T	XP_016865399.1:n.*29C>T
NM_001127496.2:c.*29C>T	NP_001120968.1:n.*29C>T
NM_001293289.2:c.*29C>T	NP_001280218.1:n.*29C>T
NM_001293290.2:c.*29C>T	NP_001280219.1:n.*29C>T
NM_030964.4:c.*29C>T	NP_112226.2:n.*29C>T
NM_001127496.3:c.*29C>T MANE Select	NP_001120968.1:n.*29C>T
NM_001293289.3:c.*29C>T	NP_001280218.1:n.*29C>T
NM_001293290.3:c.*29C>T	NP_001280219.1:n.*29C>T
NM_030964.5:c.*29C>T	NP_112226.2:n.*29C>T