Canonical Allele Identifier: CA357241292

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280825G>C (hg19) ; chr4:g.73415108G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415108G>C , CM000666.2:g.73415108G>C	GRCh38
NC_000004.11:g.74280825G>C , CM000666.1:g.74280825G>C	GRCh37
NC_000004.10:g.74499689G>C	NCBI36
NG_009291.1:g.15854G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1132G>C MANE Select	ENSP00000295897.4:p.Glu378Gln
ENST00000295897.8:c.1132G>C	ENSP00000295897.4:p.Glu378Gln
ENST00000401494.7:c.787G>C	ENSP00000384695.3:p.Glu263Gln
ENST00000415165.6:c.556G>C	ENSP00000401820.2:p.Glu186Gln
ENST00000476441.6:c.*411G>C	ENSP00000423727.1:n.*411G>C
ENST00000484992.1:n.452G>C
ENST00000503124.5:c.682G>C	ENSP00000421027.1:p.Glu228Gln
ENST00000504043.1:n.135G>C
ENST00000505649.5:n.818G>C
ENST00000509063.5:c.1132G>C	ENSP00000422784.1:p.Glu378Gln
ENST00000511370.1:c.665G>C
ENST00000621085.4:c.493G>C	ENSP00000483421.1:p.Glu165Gln
ENST00000621628.4:c.493G>C	ENSP00000480485.1:p.Glu165Gln
NM_000477.5:c.1132G>C	NP_000468.1:p.Glu378Gln
NM_000477.6:c.1132G>C	NP_000468.1:p.Glu378Gln
NM_000477.7:c.1132G>C MANE Select	NP_000468.1:p.Glu378Gln