Canonical Allele Identifier: CA1587573234

Gene: SPRY4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.142314274T= , CM000667.2:g.142314274T=	GRCh38
NC_000005.9:g.141693839T= , CM000667.1:g.141693839T=	GRCh37
NC_000005.8:g.141674023T=	NCBI36
NG_034148.1:g.15782A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000434127.3:c.835A= MANE Select	ENSP00000399468.2:p.Asn279=
ENST00000643792.1:n.1517A=
ENST00000344120.4:c.904A=	ENSP00000344967.4:p.Asn302=
ENST00000434127.2:c.835A=	ENSP00000399468.2:p.Asn279=
NM_001127496.1:c.835A=	NP_001120968.1:p.Asn279=
NM_001293289.1:c.835A=	NP_001280218.1:p.Asn279=
NM_001293290.1:c.835A=	NP_001280219.1:p.Asn279=
NM_030964.3:c.904A=	NP_112226.2:p.Asn302=
XM_011537685.1:c.904A=	XP_011535987.1:p.Asn302=
XM_011537685.3:c.904A=	XP_011535987.1:p.Asn302=
XM_017009910.2:c.835A=	XP_016865399.1:p.Asn279=
NM_001127496.2:c.835A=	NP_001120968.1:p.Asn279=
NM_001293289.2:c.835A=	NP_001280218.1:p.Asn279=
NM_001293290.2:c.835A=	NP_001280219.1:p.Asn279=
NM_030964.4:c.904A=	NP_112226.2:p.Asn302=
NM_001127496.3:c.835A= MANE Select	NP_001120968.1:p.Asn279=
NM_001293289.3:c.835A=	NP_001280218.1:p.Asn279=
NM_001293290.3:c.835A=	NP_001280219.1:p.Asn279=
NM_030964.5:c.904A=	NP_112226.2:p.Asn302=