Canonical Allele Identifier: CA2579501245
Gene: ADAMTSL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133539707T>G , CM000671.2:g.133539707T>G GRCh38
NC_000009.11:g.136404829T>G , CM000671.1:g.136404829T>G GRCh37
NC_000009.10:g.135394650T>G NCBI36
NG_009931.1:g.12544T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651351.2:c.310-64T>G MANE Select ENSP00000498961.2:n.310-64T>G
ENST00000354484.8:c.310-64T>G ENSP00000346478.4:n.310-64T>G
ENST00000393060.1:c.310-64T>G ENSP00000376780.1:n.310-64T>G
ENST00000393061.7:c.637-64T>G ENSP00000376781.3:n.637-64T>G
NM_001145320.1:c.310-64T>G NP_001138792.1:n.310-64T>G
NM_014694.3:c.310-64T>G NP_055509.2:n.310-64T>G
XM_005272237.2:c.637-64T>G XP_005272294.1:n.637-64T>G
XM_005272238.2:c.345-64T>G XP_005272295.1:n.345-64T>G
XM_005272239.2:c.310-64T>G XP_005272296.1:n.310-64T>G
XM_006717337.2:c.310-64T>G XP_006717400.1:n.310-64T>G
XM_011519241.1:c.198-64T>G XP_011517543.1:n.198-64T>G
XM_011519242.1:c.376-64T>G XP_011517544.1:n.376-64T>G
XM_005272237.3:c.637-64T>G XP_005272294.1:n.637-64T>G
XM_005272238.3:c.345-64T>G XP_005272295.1:n.345-64T>G
XM_011519241.2:c.525-64T>G XP_011517543.2:n.525-64T>G
XM_011519242.3:c.376-64T>G XP_011517544.1:n.376-64T>G
NM_014694.4:c.310-64T>G MANE Select NP_055509.2:n.310-64T>G
NM_001145320.2:c.310-64T>G NP_001138792.1:n.310-64T>G