Canonical Allele Identifier: CA1730823180
Community Standard Title: NM_005045.4(RELN):c.2702+174A>G
Gene: RELN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103629766T>C , CM000669.2:g.103629766T>C GRCh38
NC_000007.13:g.103270213T>C , CM000669.1:g.103270213T>C GRCh37
NC_000007.12:g.103057449T>C NCBI36
NG_011877.1:g.364751A>G
NG_011877.2:g.364751A>G

Transcript Alleles

HGVS Amino-acid Change
NM_005045.4:c.2702+174A>G MANE Select NP_005036.2:n.2702+174A>G
ENST00000428762.6:c.2702+174A>G MANE Select ENSP00000392423.1:n.2702+174A>G
NM_005045.3:c.2702+174A>G NP_005036.2:n.2702+174A>G
NM_173054.2:c.2702+174A>G NP_774959.1:n.2702+174A>G
NM_173054.3:c.2702+174A>G NP_774959.1:n.2702+174A>G
ENST00000343529.9:c.2702+174A>G ENSP00000345694.5:n.2702+174A>G
ENST00000424685.2:c.2702+174A>G ENSP00000388446.2:n.2702+174A>G
ENST00000424685.3:c.2702+174A>G ENSP00000388446.3:n.2702+174A>G
ENST00000428762.5:c.2702+174A>G ENSP00000392423.1:n.2702+174A>G
ENST00000473457.1:n.197+174A>G
ENST00000473457.2:n.2966+174A>G
ENST00000679867.1:n.2586+174A>G
ENST00000680706.1:n.405+174A>G
ENST00000681034.1:c.2702+174A>G ENSP00000506075.1:n.2702+174A>G