Canonical Allele Identifier: CA6092570

Gene: SYVN1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65133534T>C , CM000673.2:g.65133534T>C	GRCh38
NC_000011.9:g.64901005T>C , CM000673.1:g.64901005T>C	GRCh37
NC_000011.8:g.64657581T>C	NCBI36
NG_029713.1:g.5999A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_172230.3:c.68A>G MANE Select	NP_757385.1:p.Tyr23Cys
ENST00000377190.8:c.68A>G MANE Select	ENSP00000366395.3:p.Tyr23Cys
NM_032431.2:c.68A>G	NP_115807.1:p.Tyr23Cys
NM_032431.3:c.68A>G	NP_115807.1:p.Tyr23Cys
NM_172230.2:c.68A>G	NP_757385.1:p.Tyr23Cys
ENST00000294256.12:c.68A>G	ENSP00000294256.8:p.Tyr23Cys
ENST00000307289.10:c.68A>G	ENSP00000302035.6:p.Tyr23Cys
ENST00000377190.7:c.68A>G	ENSP00000366395.3:p.Tyr23Cys
ENST00000449943.5:n.117A>G
ENST00000526060.5:c.68A>G	ENSP00000436984.1:p.Tyr23Cys
ENST00000527142.5:c.68A>G	ENSP00000432888.1:p.Tyr23Cys
ENST00000528487.1:c.68A>G	ENSP00000431720.1:p.Tyr23Cys
ENST00000532771.5:c.15A>G
XM_011545303.1:c.68A>G	XP_011543605.1:p.Tyr23Cys
XM_011545303.3:c.68A>G	XP_011543605.1:p.Tyr23Cys