Canonical Allele Identifier: CA446909669

Gene: SPRY4

Linked Data

• MyVariant Identifiers: chr5:g.141693840C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.142314275C>G , CM000667.2:g.142314275C>G	GRCh38
NC_000005.9:g.141693840C>G , CM000667.1:g.141693840C>G	GRCh37
NC_000005.8:g.141674024C>G	NCBI36
NG_034148.1:g.15781G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434127.3:c.834G>C MANE Select	ENSP00000399468.2:p.Thr278=
ENST00000643792.1:n.1516G>C
ENST00000344120.4:c.903G>C	ENSP00000344967.4:p.Thr301=
ENST00000434127.2:c.834G>C	ENSP00000399468.2:p.Thr278=
NM_001127496.1:c.834G>C	NP_001120968.1:p.Thr278=
NM_001293289.1:c.834G>C	NP_001280218.1:p.Thr278=
NM_001293290.1:c.834G>C	NP_001280219.1:p.Thr278=
NM_030964.3:c.903G>C	NP_112226.2:p.Thr301=
XM_011537685.1:c.903G>C	XP_011535987.1:p.Thr301=
XM_011537685.3:c.903G>C	XP_011535987.1:p.Thr301=
XM_017009910.2:c.834G>C	XP_016865399.1:p.Thr278=
NM_001127496.2:c.834G>C	NP_001120968.1:p.Thr278=
NM_001293289.2:c.834G>C	NP_001280218.1:p.Thr278=
NM_001293290.2:c.834G>C	NP_001280219.1:p.Thr278=
NM_030964.4:c.903G>C	NP_112226.2:p.Thr301=
NM_001127496.3:c.834G>C MANE Select	NP_001120968.1:p.Thr278=
NM_001293289.3:c.834G>C	NP_001280218.1:p.Thr278=
NM_001293290.3:c.834G>C	NP_001280219.1:p.Thr278=
NM_030964.5:c.903G>C	NP_112226.2:p.Thr301=