Canonical Allele Identifier: CA2684156660

Gene: SLC12A9

Linked Data

• gnomAD v4: 7-100860720-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100860720_100860721insC , CM000669.2:g.100860720_100860721insC	GRCh38
NC_000007.13:g.100458342_100458343insC , CM000669.1:g.100458342_100458343insC	GRCh37
NC_000007.12:g.100296278_100296279insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354161.8:c.1219-418_1219-417insC MANE Select	ENSP00000275730.4:n.1219-418_1219-417insC
ENST00000354161.7:c.1219-418_1219-417insC	ENSP00000275730.4:n.1219-418_1219-417insC
ENST00000415287.5:c.952-418_952-417insC	ENSP00000413796.1:n.952-418_952-417insC
ENST00000416675.5:c.643-418_643-417insC	ENSP00000410692.1:n.643-418_643-417insC
ENST00000418037.5:c.427-418_427-417insC	ENSP00000406560.1:n.427-418_427-417insC
ENST00000448342.5:c.*177-292_*177-291insC	ENSP00000401583.1:n.*177-292_*177-291insC
ENST00000467972.5:n.2503-418_2503-417insC
ENST00000475623.1:n.570_571insC
ENST00000475687.5:n.2198-418_2198-417insC
ENST00000487651.5:n.1985_1986insC
ENST00000540482.5:c.1219-418_1219-417insC	ENSP00000443702.1:n.1219-418_1219-417insC
NM_001267812.1:c.1219-418_1219-417insC	NP_001254741.1:n.1219-418_1219-417insC
NM_001267814.1:c.952-418_952-417insC	NP_001254743.1:n.952-418_952-417insC
NM_020246.3:c.1219-418_1219-417insC	NP_064631.2:n.1219-418_1219-417insC
XM_005250502.2:c.952-418_952-417insC	XP_005250559.1:n.952-418_952-417insC
XM_005250504.3:c.145-418_145-417insC	XP_005250561.1:n.145-418_145-417insC
XM_006716054.2:c.952-418_952-417insC	XP_006716117.1:n.952-418_952-417insC
XM_006716055.2:c.910-418_910-417insC	XP_006716118.1:n.910-418_910-417insC
XM_011516413.1:c.784-418_784-417insC	XP_011514715.1:n.784-418_784-417insC
XM_011516414.1:c.643-418_643-417insC	XP_011514716.1:n.643-418_643-417insC
NM_001363493.1:c.1219-418_1219-417insC	NP_001350422.1:n.1219-418_1219-417insC
NM_001363494.1:c.790-418_790-417insC	NP_001350423.1:n.790-418_790-417insC
XM_005250504.4:c.145-418_145-417insC	XP_005250561.1:n.145-418_145-417insC
XM_006716055.3:c.910-418_910-417insC	XP_006716118.1:n.910-418_910-417insC
NM_020246.4:c.1219-418_1219-417insC MANE Select	NP_064631.2:n.1219-418_1219-417insC
NM_001267814.2:c.952-418_952-417insC	NP_001254743.1:n.952-418_952-417insC
NM_001363493.2:c.1219-418_1219-417insC	NP_001350422.1:n.1219-418_1219-417insC
NM_001267812.2:c.1219-418_1219-417insC	NP_001254741.1:n.1219-418_1219-417insC