Canonical Allele Identifier: CA2670937184

Gene: ALB

Linked Data

• gnomAD v4: 4-73409151-A-ACC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409152_73409153insCC , CM000666.2:g.73409152_73409153insCC	GRCh38
NC_000004.11:g.74274869_74274870insCC , CM000666.1:g.74274869_74274870insCC	GRCh37
NC_000004.10:g.74493733_74493734insCC	NCBI36
NG_009291.1:g.9898_9899insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.483-203_483-202insCC MANE Select	ENSP00000295897.4:n.483-203_483-202insCC
ENST00000295897.8:c.483-203_483-202insCC	ENSP00000295897.4:n.483-203_483-202insCC
ENST00000401494.7:c.138-203_138-202insCC	ENSP00000384695.3:n.138-203_138-202insCC
ENST00000415165.6:c.138-2844_138-2843insCC	ENSP00000401820.2:n.138-2844_138-2843insCC
ENST00000441319.5:c.489-203_489-202insCC	ENSP00000392541.1:n.489-203_489-202insCC
ENST00000476441.6:c.80-203_80-202insCC	ENSP00000423727.1:n.80-203_80-202insCC
ENST00000503124.5:c.33-203_33-202insCC	ENSP00000421027.1:n.33-203_33-202insCC
ENST00000505649.5:n.169-203_169-202insCC
ENST00000509063.5:c.483-203_483-202insCC	ENSP00000422784.1:n.483-203_483-202insCC
ENST00000514786.1:n.452-203_452-202insCC
ENST00000621085.4:c.483-203_483-202insCC	ENSP00000483421.1:n.483-203_483-202insCC
ENST00000621628.4:c.486+76_486+77insCC	ENSP00000480485.1:n.486+76_486+77insCC
NM_000477.5:c.483-203_483-202insCC	NP_000468.1:n.483-203_483-202insCC
NM_000477.6:c.483-203_483-202insCC	NP_000468.1:n.483-203_483-202insCC
NM_000477.7:c.483-203_483-202insCC MANE Select	NP_000468.1:n.483-203_483-202insCC