Canonical Allele Identifier: CA5530067

Gene: SRGN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69103944G>A , CM000672.2:g.69103944G>A	GRCh38
NC_000010.10:g.70863700G>A , CM000672.1:g.70863700G>A	GRCh37
NC_000010.9:g.70533706G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002727.4:c.301G>A MANE Select	NP_002718.2:p.Gly101Ser
ENST00000242465.4:c.301G>A MANE Select	ENSP00000242465.3:p.Gly101Ser
NM_001321053.1:c.301G>A	NP_001307982.1:p.Gly101Ser
NM_001321053.2:c.301G>A	NP_001307982.1:p.Gly101Ser
NM_001321054.1:c.133G>A	NP_001307983.1:p.Gly45Ser
NM_002727.2:c.301G>A	NP_002718.2:p.Gly101Ser
NM_002727.3:c.301G>A	NP_002718.2:p.Gly101Ser
NR_036430.1:n.239G>A
ENST00000242465.3:c.301G>A	ENSP00000242465.3:p.Gly101Ser
ENST00000462445.1:n.205G>A
XM_017016392.2:c.301G>A	XP_016871881.1:p.Gly101Ser
XM_024448064.1:c.301G>A	XP_024303832.1:p.Gly101Ser
XM_024448065.1:c.301G>A	XP_024303833.1:p.Gly101Ser
XM_024448066.1:c.301G>A	XP_024303834.1:p.Gly101Ser