Canonical Allele Identifier: CA368842867

Gene: SLC26A4

Linked Data

• MyVariant Identifiers: chr7:g.107341572T>A (hg19) ; chr7:g.107701127T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701127T>A , CM000669.2:g.107701127T>A	GRCh38
NC_000007.13:g.107341572T>A , CM000669.1:g.107341572T>A	GRCh37
NC_000007.12:g.107128808T>A	NCBI36
NG_008489.1:g.45493T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1734T>A MANE Select	ENSP00000494017.1:p.Tyr578Ter
ENST00000644846.1:c.445T>A
ENST00000265715.7:c.1734T>A	ENSP00000265715.3:p.Tyr578Ter
ENST00000480841.5:n.583T>A
ENST00000492030.2:n.91-700T>A
NM_000441.1:c.1734T>A	NP_000432.1:p.Tyr578Ter
XM_005250425.1:c.1734T>A	XP_005250482.1:p.Tyr578Ter
XM_005250425.2:c.1734T>A	XP_005250482.1:p.Tyr578Ter
XM_017012318.1:c.1656T>A	XP_016867807.1:p.Tyr552Ter
NM_000441.2:c.1734T>A MANE Select	NP_000432.1:p.Tyr578Ter