Canonical Allele Identifier: CA2694013019

Gene: TEX11

Linked Data

• gnomAD v4: X-70853431-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853431C>A , CM000685.2:g.70853431C>A	GRCh38
NC_000023.10:g.70073281C>A , CM000685.1:g.70073281C>A	GRCh37
NC_000023.9:g.69990006C>A	NCBI36
NG_012574.1:g.60287G>T
NG_012574.2:g.60287G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.325-103G>T MANE Select	ENSP00000363453.2:n.325-103G>T
ENST00000344304.3:c.370-103G>T	ENSP00000340995.3:n.370-103G>T
ENST00000374333.6:c.325-103G>T	ENSP00000363453.2:n.325-103G>T
ENST00000395889.6:c.370-103G>T	ENSP00000379226.2:n.370-103G>T
NM_001003811.1:c.370-103G>T	NP_001003811.1:n.370-103G>T
NM_031276.2:c.325-103G>T	NP_112566.2:n.325-103G>T
XM_011530994.1:c.325-103G>T	XP_011529296.1:n.325-103G>T
XM_017029649.1:c.325-103G>T	XP_016885138.1:n.325-103G>T
NM_001003811.2:c.370-103G>T	NP_001003811.1:n.370-103G>T
NM_031276.3:c.325-103G>T MANE Select	NP_112566.2:n.325-103G>T