Canonical Allele Identifier: CA357241309

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280827A>C (hg19) ; chr4:g.73415110A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415110A>C , CM000666.2:g.73415110A>C	GRCh38
NC_000004.11:g.74280827A>C , CM000666.1:g.74280827A>C	GRCh37
NC_000004.10:g.74499691A>C	NCBI36
NG_009291.1:g.15856A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1134A>C MANE Select	ENSP00000295897.4:p.Glu378Asp
ENST00000295897.8:c.1134A>C	ENSP00000295897.4:p.Glu378Asp
ENST00000401494.7:c.789A>C	ENSP00000384695.3:p.Glu263Asp
ENST00000415165.6:c.558A>C	ENSP00000401820.2:p.Glu186Asp
ENST00000476441.6:c.*413A>C	ENSP00000423727.1:n.*413A>C
ENST00000484992.1:n.454A>C
ENST00000503124.5:c.684A>C	ENSP00000421027.1:p.Glu228Asp
ENST00000504043.1:n.137A>C
ENST00000505649.5:n.820A>C
ENST00000509063.5:c.1134A>C	ENSP00000422784.1:p.Glu378Asp
ENST00000511370.1:c.667A>C
ENST00000621085.4:c.495A>C	ENSP00000483421.1:p.Glu165Asp
ENST00000621628.4:c.495A>C	ENSP00000480485.1:p.Glu165Asp
NM_000477.5:c.1134A>C	NP_000468.1:p.Glu378Asp
NM_000477.6:c.1134A>C	NP_000468.1:p.Glu378Asp
NM_000477.7:c.1134A>C MANE Select	NP_000468.1:p.Glu378Asp