Canonical Allele Identifier: CA1590838544

Gene: SLC6A7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150201758T= , CM000667.2:g.150201758T=	GRCh38
NC_000005.9:g.149581321T= , CM000667.1:g.149581321T=	GRCh37
NC_000005.8:g.149561514T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230671.7:c.858+535T= MANE Select	ENSP00000230671.2:n.858+535T=
ENST00000230671.6:c.858+535T=	ENSP00000230671.2:n.858+535T=
ENST00000524041.1:c.858+535T=	ENSP00000428200.1:n.858+535T=
NM_014228.3:c.858+535T=	NP_055043.2:n.858+535T=
NM_014228.4:c.858+535T=	NP_055043.2:n.858+535T=
XM_017009767.1:c.1212+535T=	XP_016865256.1:n.1212+535T=
XM_017009768.2:c.726+535T=	XP_016865257.1:n.726+535T=
XM_017009769.2:c.726+535T=	XP_016865258.1:n.726+535T=
XM_017009770.2:c.615+535T=	XP_016865259.1:n.615+535T=
XM_024446190.1:c.726+535T=	XP_024301958.1:n.726+535T=
XR_001742210.1:n.1232+535T=
XR_001742211.1:n.1232+535T=
XR_001742212.1:n.1121+535T=
NM_014228.5:c.858+535T= MANE Select	NP_055043.2:n.858+535T=