Canonical Allele Identifier: CA2578548304

Gene: SLC17A2

Linked Data

• gnomAD v4: 6-25918641-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.25918643del , CM000668.2:g.25918643del	GRCh38
NC_000006.11:g.25918871del , CM000668.1:g.25918871del	GRCh37
NC_000006.10:g.26026850del	NCBI36
NG_034000.1:g.17085del

Transcript Alleles

HGVS	Amino-acid change
ENST00000377850.8:c.563-69del MANE Select	ENSP00000367081.3:n.563-69del
ENST00000265425.3:c.563-69del	ENSP00000265425.3:n.563-69del
ENST00000360488.7:c.563-69del	ENSP00000353677.3:n.563-69del
ENST00000377850.7:c.563-69del	ENSP00000367081.3:n.563-69del
NM_001286123.1:c.563-69del	NP_001273052.1:n.563-69del
NM_001286125.1:c.563-69del	NP_001273054.1:n.563-69del
NM_005835.3:c.563-69del	NP_005826.1:n.563-69del
XM_005248784.2:c.563-69del	XP_005248841.1:n.563-69del
XM_006714949.2:c.563-69del	XP_006715012.1:n.563-69del
XM_006714950.1:c.494-69del	XP_006715013.1:n.494-69del
XM_006714951.1:c.563-69del	XP_006715014.1:n.563-69del
XM_011514227.1:c.563-69del	XP_011512529.1:n.563-69del
XM_006714949.3:c.563-69del	XP_006715012.1:n.563-69del
XM_006714950.2:c.494-69del	XP_006715013.1:n.494-69del
XM_017010159.1:c.494-69del	XP_016865648.1:n.494-69del
XM_017010160.1:c.563-69del	XP_016865649.1:n.563-69del
NM_001286123.3:c.563-69del MANE Select	NP_001273052.1:n.563-69del
NM_001286125.2:c.563-69del	NP_001273054.1:n.563-69del
NM_005835.4:c.563-69del	NP_005826.1:n.563-69del