Canonical Allele Identifier: CA393147816

Gene: SEMA7A

Linked Data

• MyVariant Identifiers: chr15:g.74710219A>G (hg19) ; chr15:g.74417878A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417878A>G , CM000677.2:g.74417878A>G	GRCh38
NC_000015.9:g.74710219A>G , CM000677.1:g.74710219A>G	GRCh37
NC_000015.8:g.72497272A>G	NCBI36
NG_011733.1:g.21081T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.464T>C MANE Select	ENSP00000261918.4:p.Leu155Pro
ENST00000542748.6:c.-32T>C	ENSP00000441493.1:n.-32T>C
ENST00000261918.8:c.464T>C	ENSP00000261918.4:p.Leu155Pro
ENST00000542748.5:c.-32T>C	ENSP00000441493.1:n.-32T>C
ENST00000543145.6:c.422T>C	ENSP00000438966.2:p.Leu141Pro
ENST00000567345.1:c.-32T>C	ENSP00000454365.1:n.-32T>C
NM_001146029.1:c.422T>C	NP_001139501.1:p.Leu141Pro
NM_001146030.1:c.-32T>C	NP_001139502.1:n.-32T>C
NM_003612.3:c.464T>C	NP_003603.1:p.Leu155Pro
NM_001146029.2:c.422T>C	NP_001139501.1:p.Leu141Pro
NM_001146030.2:c.-32T>C	NP_001139502.1:n.-32T>C
NM_003612.4:c.464T>C	NP_003603.1:p.Leu155Pro
NM_003612.5:c.464T>C MANE Select	NP_003603.1:p.Leu155Pro
NM_001146029.3:c.422T>C	NP_001139501.1:p.Leu141Pro
NM_001146030.3:c.-32T>C	NP_001139502.1:n.-32T>C