Canonical Allele Identifier: CA2366499461
Gene: SLC12A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46056114C= , CM000682.2:g.46056114C= GRCh38
NC_000020.10:g.44684753C= , CM000682.1:g.44684753C= GRCh37
NC_000020.9:g.44118160C= NCBI36
NG_046341.1:g.39425C=

Transcript Alleles

HGVS Amino-acid change
ENST00000243964.7:c.2788-36C= MANE Select ENSP00000243964.4:n.2788-36C=
ENST00000243964.6:c.2788-36C= ENSP00000243964.3:n.2788-36C=
ENST00000454036.6:c.2857-36C= ENSP00000387694.1:n.2857-36C=
ENST00000616201.4:c.1298-2542C= ENSP00000484585.1:n.1298-2542C=
ENST00000616202.4:c.613-2367C= ENSP00000478369.1:n.613-2367C=
ENST00000616933.4:c.*2106-36C= ENSP00000477569.1:n.*2106-36C=
ENST00000626937.2:c.510-3485C= ENSP00000485953.1:n.510-3485C=
ENST00000628413.1:n.268C=
NM_001134771.1:c.2857-36C= NP_001128243.1:n.2857-36C=
NM_020708.4:c.2788-36C= NP_065759.1:n.2788-36C=
XM_017027981.1:c.2857-36C= XP_016883470.1:n.2857-36C=
NM_001134771.2:c.2857-36C= NP_001128243.1:n.2857-36C=
NM_020708.5:c.2788-36C= MANE Select NP_065759.1:n.2788-36C=