Canonical Allele Identifier: CA357247098

Gene: ALB

Linked Data

• gnomAD v4: 4-73420264-T-C
• MyVariant Identifiers: chr4:g.74285981T>C (hg19) ; chr4:g.73420264T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420264T>C , CM000666.2:g.73420264T>C	GRCh38
NC_000004.11:g.74285981T>C , CM000666.1:g.74285981T>C	GRCh37
NC_000004.10:g.74504845T>C	NCBI36
NG_009291.1:g.21010T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1796T>C MANE Select	ENSP00000295897.4:p.Leu599Pro
ENST00000295897.8:c.1796T>C	ENSP00000295897.4:p.Leu599Pro
ENST00000401494.7:c.1451T>C	ENSP00000384695.3:p.Leu484Pro
ENST00000415165.6:c.1220T>C	ENSP00000401820.2:p.Leu407Pro
ENST00000476441.6:c.*1075T>C	ENSP00000423727.1:n.*1075T>C
ENST00000495173.1:n.104T>C
ENST00000503124.5:c.1346T>C	ENSP00000421027.1:p.Leu449Pro
ENST00000505649.5:n.1343T>C
ENST00000508932.5:n.186T>C
ENST00000509063.5:c.1785+625T>C	ENSP00000422784.1:n.1785+625T>C
ENST00000511370.1:c.1329T>C
ENST00000621085.4:c.1157T>C	ENSP00000483421.1:p.Leu386Pro
ENST00000621628.4:c.1157T>C	ENSP00000480485.1:p.Leu386Pro
NM_000477.5:c.1796T>C	NP_000468.1:p.Leu599Pro
NM_000477.6:c.1796T>C	NP_000468.1:p.Leu599Pro
NM_000477.7:c.1796T>C MANE Select	NP_000468.1:p.Leu599Pro