Canonical Allele Identifier: CA1105071713

Gene: SLC12A9

Linked Data

• gnomAD v3: 7-100860464-T-G
• gnomAD v4: 7-100860464-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100860464T>G , CM000669.2:g.100860464T>G	GRCh38
NC_000007.13:g.100458086T>G , CM000669.1:g.100458086T>G	GRCh37
NC_000007.12:g.100296022T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354161.8:c.1218+232T>G MANE Select	ENSP00000275730.4:n.1218+232T>G
ENST00000354161.7:c.1218+232T>G	ENSP00000275730.4:n.1218+232T>G
ENST00000415287.5:c.951+232T>G	ENSP00000413796.1:n.951+232T>G
ENST00000416675.5:c.642+232T>G	ENSP00000410692.1:n.642+232T>G
ENST00000418037.5:c.426+232T>G	ENSP00000406560.1:n.426+232T>G
ENST00000448342.5:c.*176+232T>G	ENSP00000401583.1:n.*176+232T>G
ENST00000467972.5:n.2502+232T>G
ENST00000475623.1:n.367-53T>G
ENST00000475687.5:n.2197+232T>G
ENST00000487651.5:n.1729T>G
ENST00000497958.5:n.840T>G
ENST00000540482.5:c.1218+232T>G	ENSP00000443702.1:n.1218+232T>G
NM_001267812.1:c.1218+232T>G	NP_001254741.1:n.1218+232T>G
NM_001267814.1:c.951+232T>G	NP_001254743.1:n.951+232T>G
NM_020246.3:c.1218+232T>G	NP_064631.2:n.1218+232T>G
XM_005250502.2:c.951+232T>G	XP_005250559.1:n.951+232T>G
XM_005250504.3:c.144+232T>G	XP_005250561.1:n.144+232T>G
XM_006716054.2:c.951+232T>G	XP_006716117.1:n.951+232T>G
XM_006716055.2:c.909+232T>G	XP_006716118.1:n.909+232T>G
XM_011516413.1:c.783+232T>G	XP_011514715.1:n.783+232T>G
XM_011516414.1:c.642+232T>G	XP_011514716.1:n.642+232T>G
NM_001363493.1:c.1218+232T>G	NP_001350422.1:n.1218+232T>G
NM_001363494.1:c.789+232T>G	NP_001350423.1:n.789+232T>G
XM_005250504.4:c.144+232T>G	XP_005250561.1:n.144+232T>G
XM_006716055.3:c.909+232T>G	XP_006716118.1:n.909+232T>G
NM_020246.4:c.1218+232T>G MANE Select	NP_064631.2:n.1218+232T>G
NM_001267814.2:c.951+232T>G	NP_001254743.1:n.951+232T>G
NM_001363493.2:c.1218+232T>G	NP_001350422.1:n.1218+232T>G
NM_001267812.2:c.1218+232T>G	NP_001254741.1:n.1218+232T>G