Canonical Allele Identifier: CA2670966846

Gene: ALB

Linked Data

• gnomAD v4: 4-73420417-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420417_73420418insT , CM000666.2:g.73420417_73420418insT	GRCh38
NC_000004.11:g.74286134_74286135insT , CM000666.1:g.74286134_74286135insT	GRCh37
NC_000004.10:g.74504998_74504999insT	NCBI36
NG_009291.1:g.21163_21164insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.*23+96_*23+97insT MANE Select	ENSP00000295897.4:n.*23+96_*23+97insT
ENST00000295897.8:c.*23+96_*23+97insT	ENSP00000295897.4:n.*23+96_*23+97insT
ENST00000401494.7:c.*23+96_*23+97insT	ENSP00000384695.3:n.*23+96_*23+97insT
ENST00000415165.6:c.*23+96_*23+97insT	ENSP00000401820.2:n.*23+96_*23+97insT
ENST00000476441.6:c.*1132+96_*1132+97insT	ENSP00000423727.1:n.*1132+96_*1132+97insT
ENST00000495173.1:n.161+96_161+97insT
ENST00000503124.5:c.*23+96_*23+97insT	ENSP00000421027.1:n.*23+96_*23+97insT
ENST00000505649.5:n.1400+96_1400+97insT
ENST00000508932.5:n.243+96_243+97insT
ENST00000509063.5:c.1786-675_1786-674insT	ENSP00000422784.1:n.1786-675_1786-674insT
ENST00000511370.1:c.1386+96_1386+97insT
ENST00000621085.4:c.*23+96_*23+97insT	ENSP00000483421.1:n.*23+96_*23+97insT
ENST00000621628.4:c.*23+96_*23+97insT	ENSP00000480485.1:n.*23+96_*23+97insT
NM_000477.5:c.*23+96_*23+97insT	NP_000468.1:n.*23+96_*23+97insT
NM_000477.6:c.*23+96_*23+97insT	NP_000468.1:n.*23+96_*23+97insT
NM_000477.7:c.*23+96_*23+97insT MANE Select	NP_000468.1:n.*23+96_*23+97insT