Canonical Allele Identifier: CA1732750890

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107709791_107709792delinsTA , CM000669.2:g.107709791_107709792delinsTA	GRCh38
NC_000007.13:g.107350236_107350237delinsTA , CM000669.1:g.107350236_107350237delinsTA	GRCh37
NC_000007.12:g.107137472_107137473delinsTA	NCBI36
NG_008489.1:g.54157_54158delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2090-263_2090-262delinsTA MANE Select	ENSP00000494017.1:n.2090-263_2090-262delinsTA
ENST00000644846.1:c.746-263_746-262delinsTA
ENST00000265715.7:c.2090-263_2090-262delinsTA	ENSP00000265715.3:n.2090-263_2090-262delinsTA
ENST00000492030.2:n.377-364_377-363delinsTA
NM_000441.1:c.2090-263_2090-262delinsTA	NP_000432.1:n.2090-263_2090-262delinsTA
XM_005250425.1:c.2090-263_2090-262delinsTA	XP_005250482.1:n.2090-263_2090-262delinsTA
XM_005250425.2:c.2090-263_2090-262delinsTA	XP_005250482.1:n.2090-263_2090-262delinsTA
XM_017012318.1:c.2012-263_2012-262delinsTA	XP_016867807.1:n.2012-263_2012-262delinsTA
NM_000441.2:c.2090-263_2090-262delinsTA MANE Select	NP_000432.1:n.2090-263_2090-262delinsTA