Canonical Allele Identifier: CA850340750

Gene: ADRA1A

Linked Data

• dbSNP Id: rs1325384534
• MyVariant Identifiers: chr8:g.26724262A>T (hg19) ; chr8:g.26866745A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.26866745A>T , CM000670.2:g.26866745A>T	GRCh38
NC_000008.10:g.26724262A>T , CM000670.1:g.26724262A>T	GRCh37
NC_000008.9:g.26780179A>T	NCBI36
NG_029395.1:g.3661T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000380573.4:c.-687+191T>A MANE Select	ENSP00000369947.3:n.-687+191T>A
ENST00000380573.3:c.-687+191T>A	ENSP00000369947.3:n.-687+191T>A
XM_005273414.3:c.-687+191T>A	XP_005273471.1:n.-687+191T>A
XM_006716292.2:c.-687+191T>A	XP_006716355.1:n.-687+191T>A
XM_006716293.2:c.-687+191T>A	XP_006716356.1:n.-687+191T>A
XM_011544411.1:c.-687+191T>A	XP_011542713.1:n.-687+191T>A
XM_011544412.1:c.-687+191T>A	XP_011542714.1:n.-687+191T>A
NM_000680.3:c.-687+191T>A	NP_000671.2:n.-687+191T>A
XM_006716292.3:c.-687+191T>A	XP_006716355.1:n.-687+191T>A
XM_006716293.4:c.-687+191T>A	XP_006716356.1:n.-687+191T>A
XM_011544411.2:c.-687+191T>A	XP_011542713.1:n.-687+191T>A
XM_011544412.3:c.-687+191T>A	XP_011542714.1:n.-687+191T>A
XM_017013094.1:c.-687+191T>A	XP_016868583.1:n.-687+191T>A
XM_017013095.1:c.-687+191T>A	XP_016868584.1:n.-687+191T>A
XM_017013096.1:c.-687+191T>A	XP_016868585.1:n.-687+191T>A
XR_001745476.1:n.335+191T>A
XR_001745477.1:n.335+191T>A
NM_000680.4:c.-687+191T>A MANE Select	NP_000671.2:n.-687+191T>A