Canonical Allele Identifier: CA1732759043
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701779A= , CM000669.2:g.107701779A= GRCh38
NC_000007.13:g.107342224A= , CM000669.1:g.107342224A= GRCh37
NC_000007.12:g.107129460A= NCBI36
NG_008489.1:g.46145A=

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1804-48A= MANE Select ENSP00000494017.1:n.1804-48A=
ENST00000644846.1:c.515-48A=
ENST00000265715.7:c.1804-48A= ENSP00000265715.3:n.1804-48A=
ENST00000480841.5:n.653-48A=
ENST00000492030.2:n.91-48A=
NM_000441.1:c.1804-48A= NP_000432.1:n.1804-48A=
XM_005250425.1:c.1804-48A= XP_005250482.1:n.1804-48A=
XM_005250425.2:c.1804-48A= XP_005250482.1:n.1804-48A=
XM_017012318.1:c.1726-48A= XP_016867807.1:n.1726-48A=
NM_000441.2:c.1804-48A= MANE Select NP_000432.1:n.1804-48A=