Canonical Allele Identifier: CA272790024

Gene: SEMA7A

Linked Data

• dbSNP Id: rs551697827
• gnomAD v3: 15-74418166-G-A
• gnomAD v4: 15-74418166-G-A
• MyVariant Identifiers: chr15:g.74710507G>A (hg19) ; chr15:g.74418166G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74418166G>A , CM000677.2:g.74418166G>A	GRCh38
NC_000015.9:g.74710507G>A , CM000677.1:g.74710507G>A	GRCh37
NC_000015.8:g.72497560G>A	NCBI36
NG_011733.1:g.20793C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261918.9:c.372+102C>T MANE Select	ENSP00000261918.4:n.372+102C>T
ENST00000542748.6:c.-124+102C>T	ENSP00000441493.1:n.-124+102C>T
ENST00000261918.8:c.372+102C>T	ENSP00000261918.4:n.372+102C>T
ENST00000542748.5:c.-124+102C>T	ENSP00000441493.1:n.-124+102C>T
ENST00000543145.6:c.331-197C>T	ENSP00000438966.2:n.331-197C>T
ENST00000567345.1:c.-124+102C>T	ENSP00000454365.1:n.-124+102C>T
NM_001146029.1:c.331-197C>T	NP_001139501.1:n.331-197C>T
NM_001146030.1:c.-124+102C>T	NP_001139502.1:n.-124+102C>T
NM_003612.3:c.372+102C>T	NP_003603.1:n.372+102C>T
NM_001146029.2:c.331-197C>T	NP_001139501.1:n.331-197C>T
NM_001146030.2:c.-124+102C>T	NP_001139502.1:n.-124+102C>T
NM_003612.4:c.372+102C>T	NP_003603.1:n.372+102C>T
NM_003612.5:c.372+102C>T MANE Select	NP_003603.1:n.372+102C>T
NM_001146029.3:c.331-197C>T	NP_001139501.1:n.331-197C>T
NM_001146030.3:c.-124+102C>T	NP_001139502.1:n.-124+102C>T