Canonical Allele Identifier: CA2638707400

Gene: SGCA

Linked Data

• gnomAD v4: 17-50169925-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50169925G>C , CM000679.2:g.50169925G>C	GRCh38
NC_000017.10:g.48247286G>C , CM000679.1:g.48247286G>C	GRCh37
NC_000017.9:g.45602285G>C	NCBI36
NG_008889.1:g.8921G>C , LRG_203:g.8921G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.598-218G>C	ENSP00000422030.2:n.598-218G>C
ENST00000511303.6:n.310-715G>C
ENST00000512526.2:c.576-715G>C	ENSP00000426606.2:n.576-715G>C
ENST00000682109.1:c.628-218G>C	ENSP00000508041.1:n.628-218G>C
ENST00000683226.1:n.1128G>C
ENST00000683294.1:c.748-139G>C	ENSP00000508134.1:n.748-139G>C
ENST00000262018.8:c.748-218G>C MANE Select	ENSP00000262018.3:n.748-218G>C
ENST00000262018.7:c.748-218G>C	ENSP00000262018.3:n.748-218G>C
ENST00000344627.10:c.585-715G>C	ENSP00000345522.6:n.585-715G>C
ENST00000502555.5:c.*1077G>C	ENSP00000422817.1:n.*1077G>C
ENST00000504073.1:c.65-218G>C
ENST00000511303.5:c.306-715G>C	ENSP00000426104.1:n.306-715G>C
ENST00000512526.1:c.420-715G>C
ENST00000513821.5:c.747+671G>C	ENSP00000426571.1:n.747+671G>C
ENST00000513942.5:n.376-715G>C
NM_000023.2:c.748-218G>C , LRG_203t1:c.748-218G>C	NP_000014.1:n.748-218G>C
NM_001135697.1:c.585-715G>C	NP_001129169.1:n.585-715G>C
XM_011525120.1:c.748-218G>C	XP_011523422.1:n.748-218G>C
XM_011525121.1:c.598-218G>C	XP_011523423.1:n.598-218G>C
XM_011525122.1:c.747+671G>C	XP_011523424.1:n.747+671G>C
XM_011525123.1:c.585-715G>C	XP_011523425.1:n.585-715G>C
XM_011525124.1:c.442-218G>C	XP_011523426.1:n.442-218G>C
XR_934517.1:n.813+671G>C
NM_000023.3:c.748-218G>C	NP_000014.1:n.748-218G>C
NM_001135697.2:c.585-715G>C	NP_001129169.1:n.585-715G>C
NR_135553.1:n.803+671G>C
XM_011525120.2:c.910-218G>C	XP_011523422.2:n.910-218G>C
XM_011525121.2:c.760-218G>C	XP_011523423.2:n.760-218G>C
XM_011525122.2:c.909+671G>C	XP_011523424.2:n.909+671G>C
XM_011525123.2:c.747-715G>C	XP_011523425.2:n.747-715G>C
XM_011525124.2:c.442-218G>C	XP_011523426.1:n.442-218G>C
XM_024450873.1:c.442-218G>C	XP_024306641.1:n.442-218G>C
XR_002958056.1:n.1266-139G>C
NM_000023.4:c.748-218G>C MANE Select	NP_000014.1:n.748-218G>C
NM_001135697.3:c.585-715G>C	NP_001129169.1:n.585-715G>C
NR_135553.2:n.783+671G>C