Canonical Allele Identifier: CA5530051

Gene: SRGN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69103897G>A , CM000672.2:g.69103897G>A	GRCh38
NC_000010.10:g.70863653G>A , CM000672.1:g.70863653G>A	GRCh37
NC_000010.9:g.70533659G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002727.4:c.254G>A MANE Select	NP_002718.2:p.Arg85His
ENST00000242465.4:c.254G>A MANE Select	ENSP00000242465.3:p.Arg85His
NM_001321053.1:c.254G>A	NP_001307982.1:p.Arg85His
NM_001321053.2:c.254G>A	NP_001307982.1:p.Arg85His
NM_001321054.1:c.86G>A	NP_001307983.1:p.Arg29His
NM_002727.2:c.254G>A	NP_002718.2:p.Arg85His
NM_002727.3:c.254G>A	NP_002718.2:p.Arg85His
NR_036430.1:n.192G>A
ENST00000242465.3:c.254G>A	ENSP00000242465.3:p.Arg85His
ENST00000462445.1:n.158G>A
XM_017016392.2:c.254G>A	XP_016871881.1:p.Arg85His
XM_024448064.1:c.254G>A	XP_024303832.1:p.Arg85His
XM_024448065.1:c.254G>A	XP_024303833.1:p.Arg85His
XM_024448066.1:c.254G>A	XP_024303834.1:p.Arg85His