Canonical Allele Identifier: CA2715529049

Gene: SLC26A4

Linked Data

• dbSNP Id: rs2129309294

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107663717_107663718insTTG , CM000669.2:g.107663717_107663718insTTG	GRCh38
NC_000007.13:g.107304162_107304163insTTG , CM000669.1:g.107304162_107304163insTTG	GRCh37
NC_000007.12:g.107091398_107091399insTTG	NCBI36
NG_008489.1:g.8083_8084insTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.304+282_304+283insTTG MANE Select	ENSP00000494017.1:n.304+282_304+283insTTG
ENST00000265715.7:c.304+282_304+283insTTG	ENSP00000265715.3:n.304+282_304+283insTTG
ENST00000440056.1:c.304+282_304+283insTTG	ENSP00000394760.1:n.304+282_304+283insTTG
NM_000441.1:c.304+282_304+283insTTG	NP_000432.1:n.304+282_304+283insTTG
XM_005250425.1:c.304+282_304+283insTTG	XP_005250482.1:n.304+282_304+283insTTG
XM_006716025.2:c.304+282_304+283insTTG	XP_006716088.1:n.304+282_304+283insTTG
XM_005250425.2:c.304+282_304+283insTTG	XP_005250482.1:n.304+282_304+283insTTG
XM_006716025.3:c.304+282_304+283insTTG	XP_006716088.1:n.304+282_304+283insTTG
XM_017012318.1:c.304+282_304+283insTTG	XP_016867807.1:n.304+282_304+283insTTG
NM_000441.2:c.304+282_304+283insTTG MANE Select	NP_000432.1:n.304+282_304+283insTTG