Canonical Allele Identifier: CA8643691

Gene: SGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50167417C>T , CM000679.2:g.50167417C>T	GRCh38
NC_000017.10:g.48244778C>T , CM000679.1:g.48244778C>T	GRCh37
NC_000017.9:g.45599777C>T	NCBI36
NG_008889.1:g.6413C>T , LRG_203:g.6413C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.87C>T	ENSP00000422030.2:p.His29=
ENST00000511303.6:n.38-530C>T
ENST00000512526.2:c.87C>T	ENSP00000426606.2:p.His29=
ENST00000682109.1:c.38-165C>T	ENSP00000508041.1:n.38-165C>T
ENST00000683294.1:c.87C>T	ENSP00000508134.1:p.His29=
ENST00000262018.8:c.87C>T MANE Select	ENSP00000262018.3:p.His29=
ENST00000262018.7:c.87C>T	ENSP00000262018.3:p.His29=
ENST00000344627.10:c.87C>T	ENSP00000345522.6:p.His29=
ENST00000502555.5:c.87C>T	ENSP00000422817.1:p.His29=
ENST00000511303.5:c.34-530C>T	ENSP00000426104.1:n.34-530C>T
ENST00000513821.5:c.87C>T	ENSP00000426571.1:p.His29=
ENST00000513942.5:n.104-530C>T
ENST00000514934.1:c.146C>T	ENSP00000423168.1:p.Thr49Ile
NM_000023.2:c.87C>T , LRG_203t1:c.87C>T	NP_000014.1:p.His29=
NM_001135697.1:c.87C>T	NP_001129169.1:p.His29=
XM_011525120.1:c.87C>T	XP_011523422.1:p.His29=
XM_011525121.1:c.87C>T	XP_011523423.1:p.His29=
XM_011525122.1:c.87C>T	XP_011523424.1:p.His29=
XM_011525123.1:c.87C>T	XP_011523425.1:p.His29=
XM_011525124.1:c.-65C>T	XP_011523426.1:n.-65C>T
XR_934517.1:n.153C>T
NM_000023.3:c.87C>T	NP_000014.1:p.His29=
NM_001135697.2:c.87C>T	NP_001129169.1:p.His29=
NR_135553.1:n.143C>T
XM_011525120.2:c.249C>T	XP_011523422.2:p.His83=
XM_011525121.2:c.249C>T	XP_011523423.2:p.His83=
XM_011525122.2:c.249C>T	XP_011523424.2:p.His83=
XM_011525123.2:c.249C>T	XP_011523425.2:p.His83=
XM_011525124.2:c.-65C>T	XP_011523426.1:n.-65C>T
XM_024450873.1:c.-65C>T	XP_024306641.1:n.-65C>T
XR_002958056.1:n.605C>T
NM_000023.4:c.87C>T MANE Select	NP_000014.1:p.His29=
NM_001135697.3:c.87C>T	NP_001129169.1:p.His29=
NR_135553.2:n.123C>T