Canonical Allele Identifier: CA1732747433

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107689230_107689235delinsTATAGG , CM000669.2:g.107689230_107689235delinsTATAGG	GRCh38
NC_000007.13:g.107329675_107329680delinsTATAGG , CM000669.1:g.107329675_107329680delinsTATAGG	GRCh37
NC_000007.12:g.107116911_107116916delinsTATAGG	NCBI36
NG_008489.1:g.33596_33601delinsTATAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1149+30_1149+35delinsTATAGG MANE Select	ENSP00000494017.1:n.1149+30_1149+35delinsTATAGG
ENST00000265715.7:c.1149+30_1149+35delinsTATAGG	ENSP00000265715.3:n.1149+30_1149+35delinsTATAGG
NM_000441.1:c.1149+30_1149+35delinsTATAGG	NP_000432.1:n.1149+30_1149+35delinsTATAGG
XM_005250425.1:c.1149+30_1149+35delinsTATAGG	XP_005250482.1:n.1149+30_1149+35delinsTATAGG
XM_006716025.2:c.1149+30_1149+35delinsTATAGG	XP_006716088.1:n.1149+30_1149+35delinsTATAGG
XM_005250425.2:c.1149+30_1149+35delinsTATAGG	XP_005250482.1:n.1149+30_1149+35delinsTATAGG
XM_006716025.3:c.1149+30_1149+35delinsTATAGG	XP_006716088.1:n.1149+30_1149+35delinsTATAGG
XM_017012318.1:c.1149+30_1149+35delinsTATAGG	XP_016867807.1:n.1149+30_1149+35delinsTATAGG
NM_000441.2:c.1149+30_1149+35delinsTATAGG MANE Select	NP_000432.1:n.1149+30_1149+35delinsTATAGG