Canonical Allele Identifier: CA1732758984

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701699T= , CM000669.2:g.107701699T=	GRCh38
NC_000007.13:g.107342144T= , CM000669.1:g.107342144T=	GRCh37
NC_000007.12:g.107129380T=	NCBI36
NG_008489.1:g.46065T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1804-128T= MANE Select	ENSP00000494017.1:n.1804-128T=
ENST00000644846.1:c.515-128T=
ENST00000265715.7:c.1804-128T=	ENSP00000265715.3:n.1804-128T=
ENST00000480841.5:n.653-128T=
ENST00000492030.2:n.91-128T=
NM_000441.1:c.1804-128T=	NP_000432.1:n.1804-128T=
XM_005250425.1:c.1804-128T=	XP_005250482.1:n.1804-128T=
XM_005250425.2:c.1804-128T=	XP_005250482.1:n.1804-128T=
XM_017012318.1:c.1726-128T=	XP_016867807.1:n.1726-128T=
NM_000441.2:c.1804-128T= MANE Select	NP_000432.1:n.1804-128T=