Canonical Allele Identifier: CA357240577

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74279185A>T (hg19) ; chr4:g.73413468A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413468A>T , CM000666.2:g.73413468A>T	GRCh38
NC_000004.11:g.74279185A>T , CM000666.1:g.74279185A>T	GRCh37
NC_000004.10:g.74498049A>T	NCBI36
NG_009291.1:g.14214A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.892A>T MANE Select	ENSP00000295897.4:p.Lys298Ter
ENST00000295897.8:c.892A>T	ENSP00000295897.4:p.Lys298Ter
ENST00000401494.7:c.547A>T	ENSP00000384695.3:p.Lys183Ter
ENST00000415165.6:c.316A>T	ENSP00000401820.2:p.Lys106Ter
ENST00000476441.6:c.*171A>T	ENSP00000423727.1:n.*171A>T
ENST00000484992.1:n.212A>T
ENST00000503124.5:c.442A>T	ENSP00000421027.1:p.Lys148Ter
ENST00000505649.5:n.578A>T
ENST00000509063.5:c.892A>T	ENSP00000422784.1:p.Lys298Ter
ENST00000511370.1:c.425A>T
ENST00000621085.4:c.491-1638A>T	ENSP00000483421.1:n.491-1638A>T
ENST00000621628.4:c.487-1634A>T	ENSP00000480485.1:n.487-1634A>T
NM_000477.5:c.892A>T	NP_000468.1:p.Lys298Ter
NM_000477.6:c.892A>T	NP_000468.1:p.Lys298Ter
NM_000477.7:c.892A>T MANE Select	NP_000468.1:p.Lys298Ter