Canonical Allele Identifier: CA350072855
Gene: ADAM23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206609994G>C , CM000664.2:g.206609994G>C GRCh38
NC_000002.11:g.207474718G>C , CM000664.1:g.207474718G>C GRCh37
NC_000002.10:g.207182963G>C NCBI36
NG_029874.2:g.171351G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264377.8:c.2444G>C MANE Select ENSP00000264377.3:p.Gly815Ala
ENST00000264377.7:c.2444G>C ENSP00000264377.3:p.Gly815Ala
ENST00000374415.7:c.2450+4114G>C ENSP00000363536.3:n.2450+4114G>C
ENST00000444281.1:c.184-7585G>C
NM_003812.3:c.2444G>C NP_003803.1:p.Gly815Ala
XM_005246932.2:c.2360-7585G>C XP_005246989.1:n.2360-7585G>C
XM_011512086.1:c.2450+4114G>C XP_011510388.1:n.2450+4114G>C
XM_005246932.3:c.2360-7585G>C XP_005246989.1:n.2360-7585G>C
XM_011512086.2:c.2450+4114G>C XP_011510388.1:n.2450+4114G>C
NM_003812.4:c.2444G>C MANE Select NP_003803.1:p.Gly815Ala