Canonical Allele Identifier: CA2534772941
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701627_107701628insATGGA , CM000669.2:g.107701627_107701628insATGGA GRCh38
NC_000007.13:g.107342072_107342073insATGGA , CM000669.1:g.107342072_107342073insATGGA GRCh37
NC_000007.12:g.107129308_107129309insATGGA NCBI36
NG_008489.1:g.45993_45994insATGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1804-200_1804-199insATGGA MANE Select ENSP00000494017.1:n.1804-200_1804-199insATGGA
ENST00000644846.1:c.515-200_515-199insATGGA
ENST00000265715.7:c.1804-200_1804-199insATGGA ENSP00000265715.3:n.1804-200_1804-199insATGGA
ENST00000480841.5:n.653-200_653-199insATGGA
ENST00000492030.2:n.91-200_91-199insATGGA
NM_000441.1:c.1804-200_1804-199insATGGA NP_000432.1:n.1804-200_1804-199insATGGA
XM_005250425.1:c.1804-200_1804-199insATGGA XP_005250482.1:n.1804-200_1804-199insATGGA
XM_005250425.2:c.1804-200_1804-199insATGGA XP_005250482.1:n.1804-200_1804-199insATGGA
XM_017012318.1:c.1726-200_1726-199insATGGA XP_016867807.1:n.1726-200_1726-199insATGGA
NM_000441.2:c.1804-200_1804-199insATGGA MANE Select NP_000432.1:n.1804-200_1804-199insATGGA