Canonical Allele Identifier: CA2768691919

Gene: SPRY4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.142314182_142314185dup , CM000667.2:g.142314182_142314185dup	GRCh38
NC_000005.9:g.141693747_141693750dup , CM000667.1:g.141693747_141693750dup	GRCh37
NC_000005.8:g.141673931_141673934dup	NCBI36
NG_034148.1:g.15871_15874dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434127.3:c.*24_*27dup MANE Select	ENSP00000399468.2:n.*24_*27dup
ENST00000643792.1:n.1606_1609dup
ENST00000344120.4:c.*24_*27dup	ENSP00000344967.4:n.*24_*27dup
ENST00000434127.2:c.*24_*27dup	ENSP00000399468.2:n.*24_*27dup
NM_001127496.1:c.*24_*27dup	NP_001120968.1:n.*24_*27dup
NM_001293289.1:c.*24_*27dup	NP_001280218.1:n.*24_*27dup
NM_001293290.1:c.*24_*27dup	NP_001280219.1:n.*24_*27dup
NM_030964.3:c.*24_*27dup	NP_112226.2:n.*24_*27dup
XM_011537685.1:c.*24_*27dup	XP_011535987.1:n.*24_*27dup
XM_011537685.3:c.*24_*27dup	XP_011535987.1:n.*24_*27dup
XM_017009910.2:c.*24_*27dup	XP_016865399.1:n.*24_*27dup
NM_001127496.2:c.*24_*27dup	NP_001120968.1:n.*24_*27dup
NM_001293289.2:c.*24_*27dup	NP_001280218.1:n.*24_*27dup
NM_001293290.2:c.*24_*27dup	NP_001280219.1:n.*24_*27dup
NM_030964.4:c.*24_*27dup	NP_112226.2:n.*24_*27dup
NM_001127496.3:c.*24_*27dup MANE Select	NP_001120968.1:n.*24_*27dup
NM_001293289.3:c.*24_*27dup	NP_001280218.1:n.*24_*27dup
NM_001293290.3:c.*24_*27dup	NP_001280219.1:n.*24_*27dup
NM_030964.5:c.*24_*27dup	NP_112226.2:n.*24_*27dup