Canonical Allele Identifier: CA349364146

Gene: AGPS

Linked Data

• MyVariant Identifiers: chr2:g.178357906G>C (hg19) ; chr2:g.177493178G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177493178G>C , CM000664.2:g.177493178G>C	GRCh38
NC_000002.11:g.178357906G>C , CM000664.1:g.178357906G>C	GRCh37
NC_000002.10:g.178066152G>C	NCBI36
NG_008968.1:g.105436G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264167.11:c.1264G>C MANE Select	ENSP00000264167.4:p.Asp422His
ENST00000637633.2:c.1264G>C	ENSP00000490844.2:p.Asp422His
ENST00000642466.2:c.1264G>C	ENSP00000494433.2:p.Asp422His
ENST00000679421.1:n.2493G>C
ENST00000679459.1:c.1264G>C	ENSP00000506137.1:p.Asp422His
ENST00000679478.1:c.994G>C	ENSP00000506484.1:p.Asp332His
ENST00000679994.1:c.994G>C	ENSP00000504957.1:p.Asp332His
ENST00000680028.1:n.2628G>C
ENST00000680155.1:c.994G>C	ENSP00000505333.1:p.Asp332His
ENST00000680390.1:n.299G>C
ENST00000680705.1:n.1308G>C
ENST00000680770.1:c.1264G>C	ENSP00000505536.1:p.Asp422His
ENST00000680893.1:c.*512G>C	ENSP00000505929.1:n.*512G>C
ENST00000680910.1:n.1294G>C
ENST00000681028.1:c.994G>C	ENSP00000506323.1:p.Asp332His
ENST00000681032.1:c.*642G>C	ENSP00000505205.1:n.*642G>C
ENST00000681300.1:n.219G>C
ENST00000681449.1:c.994G>C	ENSP00000505342.1:p.Asp332His
ENST00000681565.1:c.*397G>C	ENSP00000505620.1:n.*397G>C
ENST00000681752.1:c.*1034G>C	ENSP00000504994.1:n.*1034G>C
ENST00000681891.1:n.4899G>C
ENST00000264167.8:c.1264G>C	ENSP00000264167.4:p.Asp422His
ENST00000409888.1:c.351-28151G>C	ENSP00000386688.1:n.351-28151G>C
NM_003659.3:c.1264G>C	NP_003650.1:p.Asp422His
XM_011512041.1:c.994G>C	XP_011510343.1:p.Asp332His
XM_011512042.1:c.994G>C	XP_011510344.1:p.Asp332His
XM_011512043.1:c.529G>C	XP_011510345.1:p.Asp177His
XM_011512041.2:c.994G>C	XP_011510343.1:p.Asp332His
XM_011512043.2:c.529G>C	XP_011510345.1:p.Asp177His
XR_001739007.2:n.1172G>C
NM_003659.4:c.1264G>C MANE Select	NP_003650.1:p.Asp422His