Canonical Allele Identifier: CA1732750931

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107709836_107709841delinsATTTCT , CM000669.2:g.107709836_107709841delinsATTTCT	GRCh38
NC_000007.13:g.107350281_107350286delinsATTTCT , CM000669.1:g.107350281_107350286delinsATTTCT	GRCh37
NC_000007.12:g.107137517_107137522delinsATTTCT	NCBI36
NG_008489.1:g.54202_54207delinsATTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2090-218_2090-213delinsATTTCT MANE Select	ENSP00000494017.1:n.2090-218_2090-213delinsATTTCT
ENST00000644846.1:c.746-218_746-213delinsATTTCT
ENST00000265715.7:c.2090-218_2090-213delinsATTTCT	ENSP00000265715.3:n.2090-218_2090-213delinsATTTCT
ENST00000492030.2:n.377-319_377-314delinsATTTCT
NM_000441.1:c.2090-218_2090-213delinsATTTCT	NP_000432.1:n.2090-218_2090-213delinsATTTCT
XM_005250425.1:c.2090-218_2090-213delinsATTTCT	XP_005250482.1:n.2090-218_2090-213delinsATTTCT
XM_005250425.2:c.2090-218_2090-213delinsATTTCT	XP_005250482.1:n.2090-218_2090-213delinsATTTCT
XM_017012318.1:c.2012-218_2012-213delinsATTTCT	XP_016867807.1:n.2012-218_2012-213delinsATTTCT
NM_000441.2:c.2090-218_2090-213delinsATTTCT MANE Select	NP_000432.1:n.2090-218_2090-213delinsATTTCT