Canonical Allele Identifier: CA491212827

Gene: SEMA7A

Linked Data

• MyVariant Identifiers: chr15:g.74710275C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417934C>G , CM000677.2:g.74417934C>G	GRCh38
NC_000015.9:g.74710275C>G , CM000677.1:g.74710275C>G	GRCh37
NC_000015.8:g.72497328C>G	NCBI36
NG_011733.1:g.21025G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.408G>C MANE Select	ENSP00000261918.4:p.Arg136=
ENST00000542748.6:c.-88G>C	ENSP00000441493.1:n.-88G>C
ENST00000261918.8:c.408G>C	ENSP00000261918.4:p.Arg136=
ENST00000542748.5:c.-88G>C	ENSP00000441493.1:n.-88G>C
ENST00000543145.6:c.366G>C	ENSP00000438966.2:p.Arg122=
ENST00000567345.1:c.-88G>C	ENSP00000454365.1:n.-88G>C
NM_001146029.1:c.366G>C	NP_001139501.1:p.Arg122=
NM_001146030.1:c.-88G>C	NP_001139502.1:n.-88G>C
NM_003612.3:c.408G>C	NP_003603.1:p.Arg136=
NM_001146029.2:c.366G>C	NP_001139501.1:p.Arg122=
NM_001146030.2:c.-88G>C	NP_001139502.1:n.-88G>C
NM_003612.4:c.408G>C	NP_003603.1:p.Arg136=
NM_003612.5:c.408G>C MANE Select	NP_003603.1:p.Arg136=
NM_001146029.3:c.366G>C	NP_001139501.1:p.Arg122=
NM_001146030.3:c.-88G>C	NP_001139502.1:n.-88G>C