Canonical Allele Identifier: CA576448096

Gene: SLC12A9

Linked Data

• dbSNP Id: rs1271044063
• gnomAD v2: 7-100458381-CTG-C
• gnomAD v3: 7-100860759-CTG-C
• gnomAD v4: 7-100860759-CTG-C
• MyVariant Identifiers: chr7:g.100458382_100458383del (hg19) ; chr7:g.100860760_100860761del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100860760_100860761del , CM000669.2:g.100860760_100860761del	GRCh38
NC_000007.13:g.100458382_100458383del , CM000669.1:g.100458382_100458383del	GRCh37
NC_000007.12:g.100296318_100296319del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354161.8:c.1219-378_1219-377del MANE Select	ENSP00000275730.4:n.1219-378_1219-377del
ENST00000354161.7:c.1219-378_1219-377del	ENSP00000275730.4:n.1219-378_1219-377del
ENST00000415287.5:c.952-378_952-377del	ENSP00000413796.1:n.952-378_952-377del
ENST00000416675.5:c.643-378_643-377del	ENSP00000410692.1:n.643-378_643-377del
ENST00000418037.5:c.427-378_427-377del	ENSP00000406560.1:n.427-378_427-377del
ENST00000448342.5:c.*177-252_*177-251del	ENSP00000401583.1:n.*177-252_*177-251del
ENST00000467972.5:n.2503-378_2503-377del
ENST00000475623.1:n.610_611del
ENST00000475687.5:n.2198-378_2198-377del
ENST00000487651.5:n.2025_2026del
ENST00000540482.5:c.1219-378_1219-377del	ENSP00000443702.1:n.1219-378_1219-377del
NM_001267812.1:c.1219-378_1219-377del	NP_001254741.1:n.1219-378_1219-377del
NM_001267814.1:c.952-378_952-377del	NP_001254743.1:n.952-378_952-377del
NM_020246.3:c.1219-378_1219-377del	NP_064631.2:n.1219-378_1219-377del
XM_005250502.2:c.952-378_952-377del	XP_005250559.1:n.952-378_952-377del
XM_005250504.3:c.145-378_145-377del	XP_005250561.1:n.145-378_145-377del
XM_006716054.2:c.952-378_952-377del	XP_006716117.1:n.952-378_952-377del
XM_006716055.2:c.910-378_910-377del	XP_006716118.1:n.910-378_910-377del
XM_011516413.1:c.784-378_784-377del	XP_011514715.1:n.784-378_784-377del
XM_011516414.1:c.643-378_643-377del	XP_011514716.1:n.643-378_643-377del
NM_001363493.1:c.1219-378_1219-377del	NP_001350422.1:n.1219-378_1219-377del
NM_001363494.1:c.790-378_790-377del	NP_001350423.1:n.790-378_790-377del
XM_005250504.4:c.145-378_145-377del	XP_005250561.1:n.145-378_145-377del
XM_006716055.3:c.910-378_910-377del	XP_006716118.1:n.910-378_910-377del
NM_020246.4:c.1219-378_1219-377del MANE Select	NP_064631.2:n.1219-378_1219-377del
NM_001267814.2:c.952-378_952-377del	NP_001254743.1:n.952-378_952-377del
NM_001363493.2:c.1219-378_1219-377del	NP_001350422.1:n.1219-378_1219-377del
NM_001267812.2:c.1219-378_1219-377del	NP_001254741.1:n.1219-378_1219-377del