Canonical Allele Identifier: CA451994810

Gene: NCOA7

Linked Data

• dbSNP Id: rs1567
• gnomAD v4: 6-125928768-T-C
• MyVariant Identifiers: chr6:g.126249914T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.125928768T>C , CM000668.2:g.125928768T>C	GRCh38
NC_000006.11:g.126249914T>C , CM000668.1:g.126249914T>C	GRCh37
NC_000006.10:g.126291607T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000392477.7:c.2826T>C MANE Select	ENSP00000376269.2:p.Asp942=
ENST00000229634.13:c.2481T>C	ENSP00000229634.9:p.Asp827=
ENST00000368357.7:c.2826T>C	ENSP00000357341.3:p.Asp942=
ENST00000392477.6:c.2826T>C	ENSP00000376269.2:p.Asp942=
ENST00000438495.6:c.657T>C	ENSP00000398268.2:p.Asp219=
ENST00000444128.2:c.*103T>C	ENSP00000407684.2:n.*103T>C
NM_001122842.2:c.2793T>C	NP_001116314.1:p.Asp931=
NM_001199619.1:c.2826T>C	NP_001186548.1:p.Asp942=
NM_001199620.1:c.2826T>C	NP_001186549.1:p.Asp942=
NM_001199621.1:c.2481T>C	NP_001186550.1:p.Asp827=
NM_001199622.1:c.657T>C	NP_001186551.1:p.Asp219=
NM_181782.4:c.2826T>C	NP_861447.3:p.Asp942=
XM_005266822.3:c.2826T>C	XP_005266879.1:p.Asp942=
XM_006715340.2:c.2826T>C	XP_006715403.1:p.Asp942=
XM_011535455.1:c.2826T>C	XP_011533757.1:p.Asp942=
XM_005266822.4:c.2826T>C	XP_005266879.1:p.Asp942=
XM_006715340.4:c.2826T>C	XP_006715403.1:p.Asp942=
XM_011535455.2:c.2826T>C	XP_011533757.1:p.Asp942=
XM_017010269.1:c.2826T>C	XP_016865758.1:p.Asp942=
XM_017010270.1:c.2793T>C	XP_016865759.1:p.Asp931=
XM_017010271.1:c.2793T>C	XP_016865760.1:p.Asp931=
XM_017010272.2:c.2793T>C	XP_016865761.1:p.Asp931=
XM_017010273.2:c.2793T>C	XP_016865762.1:p.Asp931=
XM_017010274.2:c.2793T>C	XP_016865763.1:p.Asp931=
XM_024446331.1:c.2826T>C	XP_024302099.1:p.Asp942=
XM_024446332.1:c.2793T>C	XP_024302100.1:p.Asp931=
XR_001743165.2:n.3073T>C
NM_181782.5:c.2826T>C MANE Select	NP_861447.3:p.Asp942=
NM_001122842.3:c.2793T>C	NP_001116314.1:p.Asp931=
NM_001199619.2:c.2826T>C	NP_001186548.1:p.Asp942=
NM_001199620.2:c.2826T>C	NP_001186549.1:p.Asp942=
NM_001199621.2:c.2481T>C	NP_001186550.1:p.Asp827=
NM_001199622.2:c.657T>C	NP_001186551.1:p.Asp219=