Canonical Allele Identifier: CA1732748362

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107690196_107690198delinsTCC , CM000669.2:g.107690196_107690198delinsTCC	GRCh38
NC_000007.13:g.107330641_107330643delinsTCC , CM000669.1:g.107330641_107330643delinsTCC	GRCh37
NC_000007.12:g.107117877_107117879delinsTCC	NCBI36
NG_008489.1:g.34562_34564delinsTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1222_1224delinsTCC MANE Select	ENSP00000494017.1:p.Ser408=
ENST00000265715.7:c.1222_1224delinsTCC	ENSP00000265715.3:p.Ser408=
NM_000441.1:c.1222_1224delinsTCC	NP_000432.1:p.Ser408=
XM_005250425.1:c.1222_1224delinsTCC	XP_005250482.1:p.Ser408=
XM_006716025.2:c.1222_1224delinsTCC	XP_006716088.1:p.Ser408=
XM_005250425.2:c.1222_1224delinsTCC	XP_005250482.1:p.Ser408=
XM_006716025.3:c.1222_1224delinsTCC	XP_006716088.1:p.Ser408=
XM_017012318.1:c.1222_1224delinsTCC	XP_016867807.1:p.Ser408=
NM_000441.2:c.1222_1224delinsTCC MANE Select	NP_000432.1:p.Ser408=