Canonical Allele Identifier: CA400179853

Gene: SGCA

Linked Data

• gnomAD v4: 17-50168415-C-T
• COSMIC: COSM5443041 ; COSM5443042
• MyVariant Identifiers: chr17:g.48245776C>T (hg19) ; chr17:g.50168415C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50168415C>T , CM000679.2:g.50168415C>T	GRCh38
NC_000017.10:g.48245776C>T , CM000679.1:g.48245776C>T	GRCh37
NC_000017.9:g.45600775C>T	NCBI36
NG_008889.1:g.7411C>T , LRG_203:g.7411C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.427C>T	ENSP00000422030.2:p.His143Tyr
ENST00000511303.6:n.152C>T
ENST00000512526.2:c.418C>T	ENSP00000426606.2:n.418C>T
ENST00000682109.1:c.307C>T	ENSP00000508041.1:p.His103Tyr
ENST00000683226.1:n.137C>T
ENST00000683294.1:c.427C>T	ENSP00000508134.1:p.His143Tyr
ENST00000262018.8:c.427C>T MANE Select	ENSP00000262018.3:p.His143Tyr
ENST00000262018.7:c.427C>T	ENSP00000262018.3:p.His143Tyr
ENST00000344627.10:c.427C>T	ENSP00000345522.6:p.His143Tyr
ENST00000502555.5:c.*86C>T	ENSP00000422817.1:n.*86C>T
ENST00000511303.5:c.148C>T	ENSP00000426104.1:p.His50Tyr
ENST00000512526.1:c.262C>T
ENST00000513821.5:c.427C>T	ENSP00000426571.1:p.His143Tyr
ENST00000513942.5:n.218C>T
ENST00000514934.1:c.*133C>T	ENSP00000423168.1:n.*133C>T
NM_000023.2:c.427C>T , LRG_203t1:c.427C>T	NP_000014.1:p.His143Tyr
NM_001135697.1:c.427C>T	NP_001129169.1:p.His143Tyr
XM_011525120.1:c.427C>T	XP_011523422.1:p.His143Tyr
XM_011525121.1:c.427C>T	XP_011523423.1:p.His143Tyr
XM_011525122.1:c.427C>T	XP_011523424.1:p.His143Tyr
XM_011525123.1:c.427C>T	XP_011523425.1:p.His143Tyr
XM_011525124.1:c.121C>T	XP_011523426.1:p.His41Tyr
XR_934517.1:n.493C>T
NM_000023.3:c.427C>T	NP_000014.1:p.His143Tyr
NM_001135697.2:c.427C>T	NP_001129169.1:p.His143Tyr
NR_135553.1:n.483C>T
XM_011525120.2:c.589C>T	XP_011523422.2:p.His197Tyr
XM_011525121.2:c.589C>T	XP_011523423.2:p.His197Tyr
XM_011525122.2:c.589C>T	XP_011523424.2:p.His197Tyr
XM_011525123.2:c.589C>T	XP_011523425.2:p.His197Tyr
XM_011525124.2:c.121C>T	XP_011523426.1:p.His41Tyr
XM_024450873.1:c.121C>T	XP_024306641.1:p.His41Tyr
XR_002958056.1:n.945C>T
NM_000023.4:c.427C>T MANE Select	NP_000014.1:p.His143Tyr
NM_001135697.3:c.427C>T	NP_001129169.1:p.His143Tyr
NR_135553.2:n.463C>T