Canonical Allele Identifier: CA2683556088

Gene: SEMA3E

Linked Data

• gnomAD v4: 7-83392471-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83392471A>G , CM000669.2:g.83392471A>G	GRCh38
NC_000007.13:g.83021787A>G , CM000669.1:g.83021787A>G	GRCh37
NC_000007.12:g.82859723A>G	NCBI36
NG_021242.1:g.261693T>C
NG_021242.2:g.261693T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.1487+84T>C	ENSP00000405052.1:n.1487+84T>C
ENST00000642232.1:c.1667+84T>C	ENSP00000494064.1:n.1667+84T>C
ENST00000643230.2:c.1667+84T>C MANE Select	ENSP00000496491.1:n.1667+84T>C
ENST00000643441.1:n.1652+84T>C
ENST00000307792.7:c.1667+84T>C	ENSP00000303212.3:n.1667+84T>C
ENST00000427262.5:c.1487+84T>C	ENSP00000405052.1:n.1487+84T>C
NM_001178129.1:c.1487+84T>C	NP_001171600.1:n.1487+84T>C
NM_012431.2:c.1667+84T>C	NP_036563.1:n.1667+84T>C
XM_011516715.1:c.1667+84T>C	XP_011515017.1:n.1667+84T>C
NM_012431.3:c.1667+84T>C MANE Select	NP_036563.1:n.1667+84T>C
NM_001178129.2:c.1487+84T>C	NP_001171600.1:n.1487+84T>C