Canonical Allele Identifier: CA1732759099

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701821G= , CM000669.2:g.107701821G=	GRCh38
NC_000007.13:g.107342266G= , CM000669.1:g.107342266G=	GRCh37
NC_000007.12:g.107129502G=	NCBI36
NG_008489.1:g.46187G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1804-6G= MANE Select	ENSP00000494017.1:n.1804-6G=
ENST00000644846.1:c.515-6G=
ENST00000265715.7:c.1804-6G=	ENSP00000265715.3:n.1804-6G=
ENST00000480841.5:n.653-6G=
ENST00000492030.2:n.91-6G=
NM_000441.1:c.1804-6G=	NP_000432.1:n.1804-6G=
XM_005250425.1:c.1804-6G=	XP_005250482.1:n.1804-6G=
XM_005250425.2:c.1804-6G=	XP_005250482.1:n.1804-6G=
XM_017012318.1:c.1726-6G=	XP_016867807.1:n.1726-6G=
NM_000441.2:c.1804-6G= MANE Select	NP_000432.1:n.1804-6G=