Canonical Allele Identifier: CA2698077085

Gene: ASPM

Linked Data

• dbSNP Id: rs2125112362

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197139760T>C , CM000663.2:g.197139760T>C	GRCh38
NC_000001.10:g.197108890T>C , CM000663.1:g.197108890T>C	GRCh37
NC_000001.9:g.195375513T>C	NCBI36
NG_015867.1:g.11935A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367409.9:c.2026+7A>G MANE Select	ENSP00000356379.4:n.2026+7A>G
ENST00000679766.1:n.2250A>G
ENST00000680112.1:n.82+7A>G
ENST00000680265.1:c.2026+7A>G	ENSP00000505384.1:n.2026+7A>G
ENST00000680710.1:c.2026+7A>G	ENSP00000506676.1:n.2026+7A>G
ENST00000681879.1:c.2026+7A>G	ENSP00000505363.1:n.2026+7A>G
ENST00000294732.11:c.2026+7A>G	ENSP00000294732.7:n.2026+7A>G
ENST00000367409.8:c.2026+7A>G	ENSP00000356379.4:n.2026+7A>G
ENST00000612785.1:c.561+3931A>G	ENSP00000479244.1:n.561+3931A>G
NM_001206846.1:c.2026+7A>G	NP_001193775.1:n.2026+7A>G
NM_018136.4:c.2026+7A>G	NP_060606.3:n.2026+7A>G
NM_018136.5:c.2026+7A>G MANE Select	NP_060606.3:n.2026+7A>G
NM_001206846.2:c.2026+7A>G	NP_001193775.1:n.2026+7A>G