Canonical Allele Identifier: CA1732750985

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107709898_107709899delinsAG , CM000669.2:g.107709898_107709899delinsAG	GRCh38
NC_000007.13:g.107350343_107350344delinsAG , CM000669.1:g.107350343_107350344delinsAG	GRCh37
NC_000007.12:g.107137579_107137580delinsAG	NCBI36
NG_008489.1:g.54264_54265delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2090-156_2090-155delinsAG MANE Select	ENSP00000494017.1:n.2090-156_2090-155delinsAG
ENST00000644846.1:c.746-156_746-155delinsAG
ENST00000265715.7:c.2090-156_2090-155delinsAG	ENSP00000265715.3:n.2090-156_2090-155delinsAG
ENST00000492030.2:n.377-257_377-256delinsAG
NM_000441.1:c.2090-156_2090-155delinsAG	NP_000432.1:n.2090-156_2090-155delinsAG
XM_005250425.1:c.2090-156_2090-155delinsAG	XP_005250482.1:n.2090-156_2090-155delinsAG
XM_005250425.2:c.2090-156_2090-155delinsAG	XP_005250482.1:n.2090-156_2090-155delinsAG
XM_017012318.1:c.2012-156_2012-155delinsAG	XP_016867807.1:n.2012-156_2012-155delinsAG
NM_000441.2:c.2090-156_2090-155delinsAG MANE Select	NP_000432.1:n.2090-156_2090-155delinsAG