Canonical Allele Identifier: CA357238392

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275200C>T (hg19) ; chr4:g.73409483C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409483C>T , CM000666.2:g.73409483C>T	GRCh38
NC_000004.11:g.74275200C>T , CM000666.1:g.74275200C>T	GRCh37
NC_000004.10:g.74494064C>T	NCBI36
NG_009291.1:g.10229C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.611C>T MANE Select	ENSP00000295897.4:p.Pro204Leu
ENST00000295897.8:c.611C>T	ENSP00000295897.4:p.Pro204Leu
ENST00000401494.7:c.266C>T	ENSP00000384695.3:p.Pro89Leu
ENST00000415165.6:c.138-2513C>T	ENSP00000401820.2:n.138-2513C>T
ENST00000476441.6:c.208C>T	ENSP00000423727.1:p.Gln70Ter
ENST00000503124.5:c.161C>T	ENSP00000421027.1:p.Pro54Leu
ENST00000505649.5:n.297C>T
ENST00000509063.5:c.611C>T	ENSP00000422784.1:p.Pro204Leu
ENST00000511370.1:c.144C>T
ENST00000621085.4:c.490+121C>T	ENSP00000483421.1:n.490+121C>T
ENST00000621628.4:c.486+407C>T	ENSP00000480485.1:n.486+407C>T
NM_000477.5:c.611C>T	NP_000468.1:p.Pro204Leu
NM_000477.6:c.611C>T	NP_000468.1:p.Pro204Leu
NM_000477.7:c.611C>T MANE Select	NP_000468.1:p.Pro204Leu