Canonical Allele Identifier: CA400179830

Gene: SGCA

Linked Data

• gnomAD v4: 17-50168404-T-C
• MyVariant Identifiers: chr17:g.48245765T>C (hg19) ; chr17:g.50168404T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50168404T>C , CM000679.2:g.50168404T>C	GRCh38
NC_000017.10:g.48245765T>C , CM000679.1:g.48245765T>C	GRCh37
NC_000017.9:g.45600764T>C	NCBI36
NG_008889.1:g.7400T>C , LRG_203:g.7400T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000504073.2:c.416T>C	ENSP00000422030.2:p.Leu139Pro
ENST00000511303.6:n.141T>C
ENST00000512526.2:c.407T>C	ENSP00000426606.2:n.407T>C
ENST00000682109.1:c.296T>C	ENSP00000508041.1:p.Leu99Pro
ENST00000683226.1:n.126T>C
ENST00000683294.1:c.416T>C	ENSP00000508134.1:p.Leu139Pro
ENST00000262018.8:c.416T>C MANE Select	ENSP00000262018.3:p.Leu139Pro
ENST00000262018.7:c.416T>C	ENSP00000262018.3:p.Leu139Pro
ENST00000344627.10:c.416T>C	ENSP00000345522.6:p.Leu139Pro
ENST00000502555.5:c.*75T>C	ENSP00000422817.1:n.*75T>C
ENST00000511303.5:c.137T>C	ENSP00000426104.1:p.Leu46Pro
ENST00000512526.1:c.251T>C
ENST00000513821.5:c.416T>C	ENSP00000426571.1:p.Leu139Pro
ENST00000513942.5:n.207T>C
ENST00000514934.1:c.*122T>C	ENSP00000423168.1:n.*122T>C
NM_000023.2:c.416T>C , LRG_203t1:c.416T>C	NP_000014.1:p.Leu139Pro
NM_001135697.1:c.416T>C	NP_001129169.1:p.Leu139Pro
XM_011525120.1:c.416T>C	XP_011523422.1:p.Leu139Pro
XM_011525121.1:c.416T>C	XP_011523423.1:p.Leu139Pro
XM_011525122.1:c.416T>C	XP_011523424.1:p.Leu139Pro
XM_011525123.1:c.416T>C	XP_011523425.1:p.Leu139Pro
XM_011525124.1:c.110T>C	XP_011523426.1:p.Leu37Pro
XR_934517.1:n.482T>C
NM_000023.3:c.416T>C	NP_000014.1:p.Leu139Pro
NM_001135697.2:c.416T>C	NP_001129169.1:p.Leu139Pro
NR_135553.1:n.472T>C
XM_011525120.2:c.578T>C	XP_011523422.2:p.Leu193Pro
XM_011525121.2:c.578T>C	XP_011523423.2:p.Leu193Pro
XM_011525122.2:c.578T>C	XP_011523424.2:p.Leu193Pro
XM_011525123.2:c.578T>C	XP_011523425.2:p.Leu193Pro
XM_011525124.2:c.110T>C	XP_011523426.1:p.Leu37Pro
XM_024450873.1:c.110T>C	XP_024306641.1:p.Leu37Pro
XR_002958056.1:n.934T>C
NM_000023.4:c.416T>C MANE Select	NP_000014.1:p.Leu139Pro
NM_001135697.3:c.416T>C	NP_001129169.1:p.Leu139Pro
NR_135553.2:n.452T>C