Canonical Allele Identifier: CA457105111

Gene: SLC26A4

Linked Data

• MyVariant Identifiers: chr7:g.107312635T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107672190T>G , CM000669.2:g.107672190T>G	GRCh38
NC_000007.13:g.107312635T>G , CM000669.1:g.107312635T>G	GRCh37
NC_000007.12:g.107099871T>G	NCBI36
NG_008489.1:g.16556T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.357T>G MANE Select	ENSP00000494017.1:p.Ser119=
ENST00000265715.7:c.357T>G	ENSP00000265715.3:p.Ser119=
ENST00000440056.1:c.357T>G	ENSP00000394760.1:p.Ser119=
NM_000441.1:c.357T>G	NP_000432.1:p.Ser119=
XM_005250425.1:c.357T>G	XP_005250482.1:p.Ser119=
XM_006716025.2:c.357T>G	XP_006716088.1:p.Ser119=
XM_005250425.2:c.357T>G	XP_005250482.1:p.Ser119=
XM_006716025.3:c.357T>G	XP_006716088.1:p.Ser119=
XM_017012318.1:c.357T>G	XP_016867807.1:p.Ser119=
NM_000441.2:c.357T>G MANE Select	NP_000432.1:p.Ser119=