Canonical Allele Identifier: CA361599257

Gene: SPRY4

Linked Data

• gnomAD v4: 5-142314268-C-G
• MyVariant Identifiers: chr5:g.141693833C>G (hg19) ; chr5:g.142314268C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.142314268C>G , CM000667.2:g.142314268C>G	GRCh38
NC_000005.9:g.141693833C>G , CM000667.1:g.141693833C>G	GRCh37
NC_000005.8:g.141674017C>G	NCBI36
NG_034148.1:g.15788G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434127.3:c.841G>C MANE Select	ENSP00000399468.2:p.Val281Leu
ENST00000643792.1:n.1523G>C
ENST00000344120.4:c.910G>C	ENSP00000344967.4:p.Val304Leu
ENST00000434127.2:c.841G>C	ENSP00000399468.2:p.Val281Leu
NM_001127496.1:c.841G>C	NP_001120968.1:p.Val281Leu
NM_001293289.1:c.841G>C	NP_001280218.1:p.Val281Leu
NM_001293290.1:c.841G>C	NP_001280219.1:p.Val281Leu
NM_030964.3:c.910G>C	NP_112226.2:p.Val304Leu
XM_011537685.1:c.910G>C	XP_011535987.1:p.Val304Leu
XM_011537685.3:c.910G>C	XP_011535987.1:p.Val304Leu
XM_017009910.2:c.841G>C	XP_016865399.1:p.Val281Leu
NM_001127496.2:c.841G>C	NP_001120968.1:p.Val281Leu
NM_001293289.2:c.841G>C	NP_001280218.1:p.Val281Leu
NM_001293290.2:c.841G>C	NP_001280219.1:p.Val281Leu
NM_030964.4:c.910G>C	NP_112226.2:p.Val304Leu
NM_001127496.3:c.841G>C MANE Select	NP_001120968.1:p.Val281Leu
NM_001293289.3:c.841G>C	NP_001280218.1:p.Val281Leu
NM_001293290.3:c.841G>C	NP_001280219.1:p.Val281Leu
NM_030964.5:c.910G>C	NP_112226.2:p.Val304Leu