Canonical Allele Identifier: CA129101662
Gene: SLC6A7 HGNC NCBI

Linked Data

dbSNP Id: rs748891598

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150201782T>G , CM000667.2:g.150201782T>G GRCh38
NC_000005.9:g.149581345T>G , CM000667.1:g.149581345T>G GRCh37
NC_000005.8:g.149561538T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000230671.7:c.858+559T>G MANE Select ENSP00000230671.2:n.858+559T>G
ENST00000230671.6:c.858+559T>G ENSP00000230671.2:n.858+559T>G
ENST00000524041.1:c.858+559T>G ENSP00000428200.1:n.858+559T>G
NM_014228.3:c.858+559T>G NP_055043.2:n.858+559T>G
NM_014228.4:c.858+559T>G NP_055043.2:n.858+559T>G
XM_017009767.1:c.1212+559T>G XP_016865256.1:n.1212+559T>G
XM_017009768.2:c.726+559T>G XP_016865257.1:n.726+559T>G
XM_017009769.2:c.726+559T>G XP_016865258.1:n.726+559T>G
XM_017009770.2:c.615+559T>G XP_016865259.1:n.615+559T>G
XM_024446190.1:c.726+559T>G XP_024301958.1:n.726+559T>G
XR_001742210.1:n.1232+559T>G
XR_001742211.1:n.1232+559T>G
XR_001742212.1:n.1121+559T>G
NM_014228.5:c.858+559T>G MANE Select NP_055043.2:n.858+559T>G