Canonical Allele Identifier: CA393147821

Gene: SEMA7A

Linked Data

• MyVariant Identifiers: chr15:g.74710220G>T (hg19) ; chr15:g.74417879G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417879G>T , CM000677.2:g.74417879G>T	GRCh38
NC_000015.9:g.74710220G>T , CM000677.1:g.74710220G>T	GRCh37
NC_000015.8:g.72497273G>T	NCBI36
NG_011733.1:g.21080C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.463C>A MANE Select	ENSP00000261918.4:p.Leu155Met
ENST00000542748.6:c.-33C>A	ENSP00000441493.1:n.-33C>A
ENST00000261918.8:c.463C>A	ENSP00000261918.4:p.Leu155Met
ENST00000542748.5:c.-33C>A	ENSP00000441493.1:n.-33C>A
ENST00000543145.6:c.421C>A	ENSP00000438966.2:p.Leu141Met
ENST00000567345.1:c.-33C>A	ENSP00000454365.1:n.-33C>A
NM_001146029.1:c.421C>A	NP_001139501.1:p.Leu141Met
NM_001146030.1:c.-33C>A	NP_001139502.1:n.-33C>A
NM_003612.3:c.463C>A	NP_003603.1:p.Leu155Met
NM_001146029.2:c.421C>A	NP_001139501.1:p.Leu141Met
NM_001146030.2:c.-33C>A	NP_001139502.1:n.-33C>A
NM_003612.4:c.463C>A	NP_003603.1:p.Leu155Met
NM_003612.5:c.463C>A MANE Select	NP_003603.1:p.Leu155Met
NM_001146029.3:c.421C>A	NP_001139501.1:p.Leu141Met
NM_001146030.3:c.-33C>A	NP_001139502.1:n.-33C>A