Canonical Allele Identifier: CA2636826893

Gene: SLC46A1

Linked Data

• gnomAD v4: 17-28405845-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28405845A>G , CM000679.2:g.28405845A>G	GRCh38
NC_000017.10:g.26732863A>G , CM000679.1:g.26732863A>G	GRCh37
NC_000017.9:g.23756990A>G	NCBI36
NG_013306.1:g.5366T>C , LRG_183:g.5366T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000612814.5:c.228+42T>C MANE Select	ENSP00000480703.1:n.228+42T>C
ENST00000581516.1:c.6+42T>C	ENSP00000462942.1:n.6+42T>C
ENST00000582590.1:n.282+42T>C
ENST00000584426.1:c.-36-377T>C	ENSP00000467416.1:n.-36-377T>C
ENST00000584995.5:c.6+42T>C	ENSP00000464190.1:n.6+42T>C
ENST00000612814.4:c.228+42T>C	ENSP00000480703.1:n.228+42T>C
ENST00000618626.1:c.228+42T>C	ENSP00000483652.1:n.228+42T>C
NM_001242366.2:c.228+42T>C	NP_001229295.1:n.228+42T>C
NM_080669.5:c.228+42T>C	NP_542400.2:n.228+42T>C
XM_005277786.2:c.228+42T>C	XP_005277843.1:n.228+42T>C
XR_934643.1:n.89+394A>G
XM_005277786.3:c.228+42T>C	XP_005277843.1:n.228+42T>C
XM_017024110.1:c.6+42T>C	XP_016879599.1:n.6+42T>C
NM_080669.6:c.228+42T>C MANE Select	NP_542400.2:n.228+42T>C
NM_001242366.3:c.228+42T>C	NP_001229295.1:n.228+42T>C