Canonical Allele Identifier: CA357241023

Gene: ALB

Linked Data

• gnomAD v4: 4-73415035-G-T
• MyVariant Identifiers: chr4:g.74280752G>T (hg19) ; chr4:g.73415035G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415035G>T , CM000666.2:g.73415035G>T	GRCh38
NC_000004.11:g.74280752G>T , CM000666.1:g.74280752G>T	GRCh37
NC_000004.10:g.74499616G>T	NCBI36
NG_009291.1:g.15781G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1059G>T MANE Select	ENSP00000295897.4:p.Met353Ile
ENST00000295897.8:c.1059G>T	ENSP00000295897.4:p.Met353Ile
ENST00000401494.7:c.714G>T	ENSP00000384695.3:p.Met238Ile
ENST00000415165.6:c.483G>T	ENSP00000401820.2:p.Met161Ile
ENST00000476441.6:c.*338G>T	ENSP00000423727.1:n.*338G>T
ENST00000484992.1:n.379G>T
ENST00000503124.5:c.609G>T	ENSP00000421027.1:p.Met203Ile
ENST00000504043.1:n.62G>T
ENST00000505649.5:n.745G>T
ENST00000509063.5:c.1059G>T	ENSP00000422784.1:p.Met353Ile
ENST00000511370.1:c.592G>T
ENST00000621085.4:c.491-71G>T	ENSP00000483421.1:n.491-71G>T
ENST00000621628.4:c.487-67G>T	ENSP00000480485.1:n.487-67G>T
NM_000477.5:c.1059G>T	NP_000468.1:p.Met353Ile
NM_000477.6:c.1059G>T	NP_000468.1:p.Met353Ile
NM_000477.7:c.1059G>T MANE Select	NP_000468.1:p.Met353Ile