Canonical Allele Identifier: CA361599283

Gene: SPRY4

Linked Data

• MyVariant Identifiers: chr5:g.141693844T>G (hg19) ; chr5:g.142314279T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.142314279T>G , CM000667.2:g.142314279T>G	GRCh38
NC_000005.9:g.141693844T>G , CM000667.1:g.141693844T>G	GRCh37
NC_000005.8:g.141674028T>G	NCBI36
NG_034148.1:g.15777A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434127.3:c.830A>C MANE Select	ENSP00000399468.2:p.His277Pro
ENST00000643792.1:n.1512A>C
ENST00000344120.4:c.899A>C	ENSP00000344967.4:p.His300Pro
ENST00000434127.2:c.830A>C	ENSP00000399468.2:p.His277Pro
NM_001127496.1:c.830A>C	NP_001120968.1:p.His277Pro
NM_001293289.1:c.830A>C	NP_001280218.1:p.His277Pro
NM_001293290.1:c.830A>C	NP_001280219.1:p.His277Pro
NM_030964.3:c.899A>C	NP_112226.2:p.His300Pro
XM_011537685.1:c.899A>C	XP_011535987.1:p.His300Pro
XM_011537685.3:c.899A>C	XP_011535987.1:p.His300Pro
XM_017009910.2:c.830A>C	XP_016865399.1:p.His277Pro
NM_001127496.2:c.830A>C	NP_001120968.1:p.His277Pro
NM_001293289.2:c.830A>C	NP_001280218.1:p.His277Pro
NM_001293290.2:c.830A>C	NP_001280219.1:p.His277Pro
NM_030964.4:c.899A>C	NP_112226.2:p.His300Pro
NM_001127496.3:c.830A>C MANE Select	NP_001120968.1:p.His277Pro
NM_001293289.3:c.830A>C	NP_001280218.1:p.His277Pro
NM_001293290.3:c.830A>C	NP_001280219.1:p.His277Pro
NM_030964.5:c.899A>C	NP_112226.2:p.His300Pro