Canonical Allele Identifier: CA383457600

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750530C>G (hg19) ; chr11:g.130880635C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880635C>G , CM000673.2:g.130880635C>G	GRCh38
NC_000011.9:g.130750530C>G , CM000673.1:g.130750530C>G	GRCh37
NC_000011.8:g.130255740C>G	NCBI36
NG_053190.1:g.40854G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2745G>C MANE Select	ENSP00000265909.4:p.Met915Ile
ENST00000265909.8:c.2745G>C	ENSP00000265909.4:p.Met915Ile
ENST00000426933.6:c.249G>C	ENSP00000413345.2:p.Met83Ile
ENST00000526579.5:n.178-924G>C
ENST00000527116.5:n.507G>C
ENST00000528555.5:c.885G>C	ENSP00000435122.1:p.Met295Ile
ENST00000530330.1:n.481G>C
ENST00000530356.5:c.885G>C	ENSP00000432307.1:p.Met295Ile
ENST00000533318.5:n.1105G>C
ENST00000534726.5:c.465G>C	ENSP00000433699.1:p.Met155Ile
NM_001301089.1:c.885G>C	NP_001288018.1:p.Met295Ile
NM_014758.2:c.2745G>C	NP_055573.2:p.Met915Ile
XM_005271546.3:c.2574-924G>C	XP_005271603.1:n.2574-924G>C
XM_011542819.1:c.2991G>C	XP_011541121.1:p.Met997Ile
XM_011542820.1:c.2979G>C	XP_011541122.1:p.Met993Ile
XM_011542821.1:c.2871G>C	XP_011541123.1:p.Met957Ile
XM_011542824.1:c.2109G>C	XP_011541126.1:p.Met703Ile
XM_011542825.1:c.1266G>C	XP_011541127.1:p.Met422Ile
XM_011542826.1:c.1131G>C	XP_011541128.1:p.Met377Ile
XM_011542827.1:c.1011G>C	XP_011541129.1:p.Met337Ile
NM_001347918.1:c.2625G>C	NP_001334847.1:p.Met875Ile
NM_001347919.1:c.2574-924G>C	NP_001334848.1:n.2574-924G>C
NM_001347922.1:c.1074G>C	NP_001334851.1:p.Met358Ile
NM_001347923.1:c.1020G>C	NP_001334852.1:p.Met340Ile
NM_001347924.1:c.765G>C	NP_001334853.1:p.Met255Ile
NM_001347925.1:c.711G>C	NP_001334854.1:p.Met237Ile
NM_001347926.1:c.714-924G>C	NP_001334855.1:n.714-924G>C
NM_001347927.1:c.465G>C	NP_001334856.1:p.Met155Ile
NR_144939.1:n.3378G>C
XM_011542820.2:c.2979G>C	XP_011541122.1:p.Met993Ile
XM_011542821.3:c.2871G>C	XP_011541123.1:p.Met957Ile
XM_011542824.2:c.2109G>C	XP_011541126.1:p.Met703Ile
XM_011542825.2:c.1266G>C	XP_011541127.1:p.Met422Ile
XM_011542826.2:c.1131G>C	XP_011541128.1:p.Met377Ile
XM_024448521.1:c.2991G>C	XP_024304289.1:p.Met997Ile
XR_001747870.1:n.3816G>C
XR_001747872.1:n.3162G>C
XR_001747873.1:n.3476G>C
NM_001301089.2:c.885G>C	NP_001288018.1:p.Met295Ile
NM_001347918.2:c.2625G>C	NP_001334847.2:p.Met875Ile
NM_001347919.2:c.2574-924G>C	NP_001334848.2:n.2574-924G>C
NM_001347920.2:c.*21141G>C	NP_001334849.2:n.*21141G>C
NM_001347922.2:c.1074G>C	NP_001334851.2:p.Met358Ile
NM_001347923.2:c.1020G>C	NP_001334852.2:p.Met340Ile
NM_001347924.2:c.765G>C	NP_001334853.1:p.Met255Ile
NM_001347925.2:c.711G>C	NP_001334854.1:p.Met237Ile
NM_001347926.2:c.714-924G>C	NP_001334855.1:n.714-924G>C
NM_001347927.2:c.465G>C	NP_001334856.1:p.Met155Ile
NM_014758.3:c.2745G>C MANE Select	NP_055573.3:p.Met915Ile
NR_144939.2:n.3370G>C