Canonical Allele Identifier: CA1143355932
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197104102_197104108delinsTTTTTTT , CM000663.2:g.197104102_197104108delinsTTTTTTT GRCh38
NC_000001.10:g.197073232_197073238delinsTTTTTTT , CM000663.1:g.197073232_197073238delinsTTTTTTT GRCh37
NC_000001.9:g.195339855_195339861delinsTTTTTTT NCBI36
NG_015867.1:g.47587_47593delinsAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.2108-7944_2108-7938delinsAAAAAAA
ENST00000367409.9:c.5143_5149delinsAAAAAAA MANE Select ENSP00000356379.4:p.Lys1715=
ENST00000680265.1:c.5143_5149delinsAAAAAAA ENSP00000505384.1:p.Lys1715=
ENST00000680710.1:c.5143_5149delinsAAAAAAA ENSP00000506676.1:p.Lys1715=
ENST00000294732.11:c.4066-7944_4066-7938delinsAAAAAAA ENSP00000294732.7:n.4066-7944_4066-7938delinsAAAAAAA
ENST00000367408.5:c.1816-7944_1816-7938delinsAAAAAAA ENSP00000356378.1:n.1816-7944_1816-7938delinsAAAAAAA
ENST00000367409.8:c.5143_5149delinsAAAAAAA ENSP00000356379.4:p.Lys1715=
ENST00000612785.1:c.562-1461_562-1455delinsAAAAAAA ENSP00000479244.1:n.562-1461_562-1455delinsAAAAAAA
NM_001206846.1:c.4066-7944_4066-7938delinsAAAAAAA NP_001193775.1:n.4066-7944_4066-7938delinsAAAAAAA
NM_018136.4:c.5143_5149delinsAAAAAAA NP_060606.3:p.Lys1715=
NM_018136.5:c.5143_5149delinsAAAAAAA MANE Select NP_060606.3:p.Lys1715=
NM_001206846.2:c.4066-7944_4066-7938delinsAAAAAAA NP_001193775.1:n.4066-7944_4066-7938delinsAAAAAAA