Canonical Allele Identifier: CA347264128

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73716902T>A (hg19) ; chr2:g.73489775T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489775T>A , CM000664.2:g.73489775T>A	GRCh38
NC_000002.11:g.73716902T>A , CM000664.1:g.73716902T>A	GRCh37
NC_000002.10:g.73570410T>A	NCBI36
NG_011690.1:g.109023T>A , LRG_741:g.109023T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7435T>A	ENSP00000507671.1:p.Ser2479Thr
ENST00000682801.1:c.7435T>A	ENSP00000507862.1:p.Ser2479Thr
ENST00000682859.1:c.7435T>A	ENSP00000508222.1:p.Ser2479Thr
ENST00000683791.1:c.827T>A
ENST00000684460.1:c.4887T>A
ENST00000684548.1:c.7435T>A	ENSP00000507421.1:p.Ser2479Thr
ENST00000684590.1:c.1882T>A	ENSP00000507376.1:p.Ser628Thr
ENST00000684656.1:c.4887T>A
ENST00000613296.6:c.7816T>A MANE Select	ENSP00000482968.1:p.Ser2606Thr
ENST00000651434.1:c.896-30000T>A
ENST00000423048.5:c.2647T>A	ENSP00000399833.1:p.Ser883Thr
ENST00000484298.5:c.7690T>A	ENSP00000478155.1:p.Ser2564Thr
ENST00000613296.4:c.7816T>A	ENSP00000482968.1:p.Ser2606Thr
ENST00000614410.4:c.7816T>A	ENSP00000479094.1:p.Ser2606Thr
ENST00000620466.4:n.1619T>A
NM_015120.4:c.7819T>A , LRG_741t1:c.7819T>A	NP_055935.4:p.Ser2607Thr
NM_001378454.1:c.7816T>A MANE Select	NP_001365383.1:p.Ser2606Thr